SNP ID | Position (GRCh38.p7) | Alleles | Variant Type | Genomic Region | Phenotype |
rs202195141 | chr15:91850866-91850868 | dupAG | Indel | LOC105370974 : Intron Variant | ND |
rs58598658 | chr13:73887726-73887733 | dupA / dupAA | Indel | KLF12 : Intron Variant | AD |
rs201013261 | chr3:64125982-64125983 | insAC | Insertion | PRICKLE2 : Intron Variant | ND |
rs200589189 | chr1:62918621-62918622 | insG | Insertion | Intergenic | AD |
rs200457189 | chr5:54269225-54269251 | delT(A)4 | Indel | ARL15 : Intron Variant | AD |
rs372540087 | chr13:46180600-46180605 | delAGA | Indel | LCP1 : Intron Variant | AD |
rs386752273 | chr11:33393606-33393607 | GG>TA | MNVMultipleNucleotideVariation | KIAA1549L : Intron Variant | AD |
rs547301762 | chr21:25413996-25413999 | dupTGCT | Indel | LINC00158 : Intron Variant | ND |
rs532723366 | chr21:24842732-24842742 | delGTCT | Indel | LOC339622 : Intron Variant | AD |
rs79139973 | chr3:164849972-164849974 | insATAA | Indel | Intergenic | AD |
rs10649162 | chr6:153299421-153299422 | dupAG | Indel | Intergenic | AD |
rs113791767 | chr15:100553925-100553926 | insT | Insertion | PRKXP1 : Non Coding Transcript Variant | AD |
rs544313 | NT_008705.16:17902530 (GRCh37.p13) | G>A | SNV | Intergenic | AD |
rs7796556 | NT_187562.1:514632 | G>A | SNV | LOC105379749 : Intron Variant | AD |
rs12745508 | chr1:247454677 | G>A / G>C | SNV | Intergenic | AD |
rs3738443 | chr1:247184887 | C>T | SNV | Intergenic | AD |
rs3120701 | chr1:246542837 | C>T | SNV | TFB2M : Intron Variant | ND |
rs2817475 | chr1:245798900 | C>T | SNV | SMYD3 : Intron Variant LOC105373270 : 2KB Upstream Variant | ND |
rs488109 | chr1:244265229 | C>G | SNV | LOC105373262 : Intron Variant | AD |
rs913992 | chr1:244151174 | C>T | SNV | Intergenic | AD |
rs6657754 | chr1:242710653 | C>A / C>T | SNV | Intergenic | AD |
rs10926828 | chr1:242710293 | T>C | SNV | Intergenic | AD |
rs1413202 | chr1:242708730 | A>C / A>G | SNV | Intergenic | AD |
rs2809985 | chr1:242399419 | A>G | SNV | PLD5 : Intron Variant | ND |
rs10926554 | chr1:241730784 | C>A | SNV | WDR64 : Intron Variant | ND |
rs9782914 | chr1:241728933 | T>C | SNV | WDR64 : Intron Variant | AD |
rs9428890 | chr1:241705047 | G>A | SNV | WDR64 : Intron Variant | AD |
rs6678986 | chr1:241521531 | A>G | SNV | FH : 2KB Upstream Variant | AD |
rs10158567 | chr1:241125210 | G>A | SNV | RGS7 : Intron Variant | AD |
rs12086317 | chr1:241100916 | A>G | SNV | RGS7 : Intron Variant | AD |
rs10926254 | chr1:240435799 | A>G | SNV | FMN2 : Intron Variant | AD |
rs10802867 | chr1:240401213 | A>G | SNV | FMN2 : Intron Variant | AD |
rs1030891 | chr2:239618071 | A>G | SNV | Intergenic | AD |
rs12080951 | chr1:239615360 | C>T | SNV | CHRM3 : Intron Variant LOC105373225 : Intron Variant | AD |
rs12135445 | chr1:239579957 | G>A | SNV | CHRM3 : Intron Variant | AD |
rs62191099 | chr2:238936057 | G>A | SNV | Intergenic | AD |
rs16837283 | chr1:238655494 | T>C | SNV | Intergenic | AD |
rs7517092 | chr1:238607926 | T>C | SNV | Intergenic | AD |
rs923542 | chr1:238396597 | C>A | SNV | LOC105373220 : Intron Variant | AD |
rs12756158 | chr1:238311294 | A>G | SNV | Intergenic | AD |
rs62197363 | chr2:238120099 | T>C | SNV | ESPNL : Intron Variant | AD |
rs13025510 | chr2:238108499 | G>A | SNV | ESPNL : Intron Variant | AD |
rs878133 | chr2:238108292 | G>A | SNV | ESPNL : Intron Variant | AD |
rs878134 | chr2:238107999 | G>T | SNV | ESPNL : Intron Variant | AD |
rs4663285 | chr2:238106193 | G>A | SNV | ESPNL : Intron Variant | AD |
rs62196019 | chr2:238106074 | G>A | SNV | ESPNL : Intron Variant | AD |
rs4663837 | chr2:238105200 | C>A / C>T | SNV | ESPNL : Intron Variant | AD |
rs34878344 | chr2:238102049 | C>A / C>T | SNV | ESPNL : Missense Variant | AD |
rs62196014 | chr2:238101526 | C>G | SNV | ESPNL : Intron Variant | AD |
rs13006807 | chr2:238099901 | C>T | SNV | ESPNL : 2KB Upstream Variant SCLY : 500B Downstream Variant UBE2F-SCLY : 500B Downstream Variant | AD |
rs41264151 | chr2:238098994 | G>A | SNV | UBE2F-SCLY : Non Coding Transcript Variant SCLY : 3 Prime UTR Variant ESPNL : 2KB Upstream Variant | AD |
rs62196004 | chr2:238097673 | G>A | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs13033964 | chr2:238096945 | G>A | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs7591078 | chr2:238096373 | C>G | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs34049050 | chr2:238089940 | A>G | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2592583 | chr2:238087119 | G>T | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2248623 | chr2:238086187 | T>G | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2326009 | chr2:238085216 | C>A | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2248824 | chr2:238084463 | T>C | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2248825 | chr2:238084404 | G>A | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2278742 | chr2:238083155 | C>T | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2249067 | chr2:238082546 | G>A | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2249077 | chr2:238082344 | T>C | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs4663836 | chr2:238078544 | A>T | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2262426 | chr2:238075856 | G>A | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2262425 | chr2:238075488 | A>G | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2252822 | chr2:238074626 | A>G | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs7601010 | chr2:238074132 | C>T | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2264166 | chr2:238072660 | C>A | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2592585 | chr2:238070980 | C>T | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2249543 | chr2:238066170 | A>G | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs821480 | chr2:238064186 | T>C | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs821482 | chr2:238062470 | T>C | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2250038 | chr2:238062302 | G>T | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2250039 | chr2:238062296 | G>A | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2250045 | chr2:238062221 | C>T | SNV | SCLY : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2243545 | chr2:238060509 | C>T | SNV | UBE2F-SCLY : Intron Variant SCLY : 2KB Upstream Variant | AD |
rs1374479 | chr2:238059384 | C>G | SNV | UBE2F-SCLY : Intron Variant SCLY : 2KB Upstream Variant | AD |
rs821484 | chr2:238059011 | A>T | SNV | UBE2F-SCLY : Intron Variant SCLY : 2KB Upstream Variant | AD |
rs843975 | chr2:238058924 | A>C | SNV | UBE2F-SCLY : Intron Variant SCLY : 2KB Upstream Variant | AD |
rs821485 | chr2:238058166 | A>G | SNV | UBE2F-SCLY : Intron Variant | AD |
rs821486 | chr2:238058050 | T>C | SNV | UBE2F-SCLY : Intron Variant | AD |
rs2264165 | chr2:238057407 | G>A | SNV | UBE2F-SCLY : Intron Variant | AD |
rs865380 | chr2:238055357 | C>G | SNV | UBE2F-SCLY : Intron Variant | AD |
rs821488 | chr2:238055115 | T>C | SNV | UBE2F-SCLY : Intron Variant | AD |
rs821490 | chr2:238051931 | G>A | SNV | UBE2F-SCLY : Intron Variant | AD |
rs6431570 | chr2:238015926 | G>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs7594965 | chr2:238002459 | C>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs10166061 | chr2:237997869 | C>T | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs10469607 | chr2:237996150 | G>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs10203101 | chr2:237994668 | C>T | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs4663276 | chr2:237990167 | G>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs10048643 | chr2:237989292 | A>G | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs10048814 | chr2:237989113 | C>T | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs11692068 | chr2:237988964 | C>T | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs11692064 | chr2:237988945 | C>G | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs4663819 | chr2:237988732 | G>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs11690668 | chr2:237988316 | C>T | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs6755573 | chr2:237986970 | G>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs7422865 | chr2:237984050 | T>C | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs6726393 | chr2:237982949 | A>G | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs7572717 | chr2:237981674 | T>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs10187736 | chr2:237978933 | C>T | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs2121472 | chr2:237976195 | C>T | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs4461215 | chr2:237975324 | G>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs6754093 | chr2:237974093 | C>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs6711485 | chr2:237974033 | A>G | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs7567199 | chr2:237971888 | G>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs10929255 | chr2:237970660 | G>A | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs1446924 | chr2:237969098 | A>G | SNV | UBE2F : Intron Variant UBE2F-SCLY : Intron Variant | AD |
rs10167252 | chr2:237963604 | T>C | SNV | Intergenic | AD |
rs1446930 | chr2:237962237 | C>T | SNV | Intergenic | AD |
rs12737847 | chr1:237782570 | T>C | SNV | RYR2 : Intron Variant | AD |
rs10495392 | chr1:237259689 | C>T | SNV | RYR2 : Intron Variant | ND |
rs7526063 | chr1:236808698 | C>T | SNV | MTR : Intron Variant | ND |
rs475488 | chr1:236658547 | G>A | SNV | Intergenic | ND |
rs7594454 | chr2:236629292 | C>T | SNV | Intergenic | AD |
rs6431476 | chr2:236609294 | T>C | SNV | LOC105373947 : Non Coding Transcript Variant | AD |
rs7565777 | chr2:236607651 | A>G | SNV | LOC105373947 : Intron Variant | AD |
rs896543 | chr2:236600564 | G>A | SNV | LOC107986001 : Intron Variant | AD |
rs6661946 | chr1:236559808 | C>T | SNV | HEATR1 : Missense Variant | ND |
rs7607774 | chr2:236520511 | G>A | SNV | Intergenic | AD |
rs11688841 | chr2:235887157 | G>A | SNV | AGAP1 : Intron Variant | AD |
rs4444469 | chr2:235339472 | C>A / C>T | SNV | Intergenic | AD |
rs4329572 | chr1:235127607 | C>A | SNV | TOMM20 : Intron Variant SNORA14B : 500B Downstream Variant LOC105379283 : Intron Variant | AD |
rs2802928 | chr1:234959184 | A>G | SNV | LOC101927851 : Intron Variant | AD |
rs2045518 | chr1:234094642 | A>G | SNV | SLC35F3 : Intron Variant | AD |
rs603217 | chr2:234022878 | G>A / G>C | SNV | Intergenic | ND |
rs12992084 | chr2:233946710 | T>C | SNV | TRPM8 : Intron Variant | AD |
rs12472151 | chr2:233944048 | G>A | SNV | TRPM8 : Intron Variant | AD |
rs12071360 | chr1:233608833 | T>C | SNV | Intergenic | CD |
rs2477859 | chr1:233145551 | T>C / T>G | SNV | PCNX2 : Intron Variant | ND |
rs7523847 | chr1:232964658 | C>A | SNV | NTPCR : Intron Variant | AD |
rs4141442 | chr1:232963129 | T>C | SNV | NTPCR : Intron Variant | AD |
rs9424490 | chr1:232886124 | C>G | SNV | LOC101927711 : Intron Variant | ND |
rs6699751 | chr1:232675683 | T>C | SNV | Intergenic | AD |
rs592557 | chr1:232354204 | C>A / C>T | SNV | Intergenic | ND |
rs10185448 | chr2:231802592 | A>G | SNV | COPS7B : Intron Variant | AD |
rs13408416 | chr2:231796358 | C>T | SNV | COPS7B : Intron Variant | AD |
rs1059595 | chr1:231522555 | A>G | SNV | Intergenic | AD |
rs6747728 | chr2:230914061 | A>G | SNV | GPR55 : Intron Variant | AD |
rs3792068 | chr2:230808510 | A>G | SNV | CAB39 : Intron Variant | AD |
rs6717266 | chr2:230748426 | G>A | SNV | CAB39 : Intron Variant | AD |
rs6711453 | chr2:230729374 | A>G | SNV | CAB39 : Intron Variant | AD |
rs13404879 | chr2:230723394 | G>T | SNV | CAB39 : Intron Variant | AD |
rs13411251 | chr2:230721625 | T>G | SNV | CAB39 : Intron Variant | AD |
rs10933355 | chr2:230717481 | G>A | SNV | CAB39 : Intron Variant | AD |
rs11682404 | chr2:230710181 | A>G | SNV | Intergenic | AD |
rs9973480 | chr2:230708669 | A>C | SNV | Intergenic | AD |
rs6712333 | chr2:230365456 | C>T | SNV | SP140L : Intron Variant | AD | ND |
rs1365773 | chr2:230144838 | C>A | SNV | Intergenic | AD |
rs7541570 | chr1:230129595 | T>C | SNV | GALNT2 : Intron Variant | AD |
rs10864699 | chr1:230128860 | G>A / G>T | SNV | GALNT2 : Intron Variant | AD |
rs12086347 | chr1:230127626 | G>A / G>T | SNV | GALNT2 : Intron Variant | AD |
rs12724775 | chr1:230111376 | G>A | SNV | GALNT2 : Intron Variant | AD |
rs12732392 | chr1:230109219 | A>G | SNV | GALNT2 : Intron Variant | AD |
rs12751815 | chr1:230106833 | C>T | SNV | GALNT2 : Intron Variant | AD |
rs12035297 | chr1:230103074 | C>T | SNV | GALNT2 : Intron Variant | AD |
rs12726525 | chr1:230099285 | G>A / G>T | SNV | GALNT2 : Intron Variant | AD |
rs910821 | chr1:230096494 | T>A | SNV | GALNT2 : Intron Variant | AD |
rs10779824 | chr1:230095509 | C>T | SNV | GALNT2 : Intron Variant | AD |
rs7574501 | chr2:229681362 | A>G | SNV | DNER : Intron Variant | AD |
rs2216249 | chr2:229680640 | T>C | SNV | DNER : Intron Variant | AD |
rs1419951 | chr2:229134886 | C>T | SNV | PID1 : Intron Variant | ND |
rs603404 | chr1:228969398 | A>G | SNV | Intergenic | AD |
rs11578798 | chr1:228355602 | T>A | SNV | OBSCN : Intron Variant | AD |
rs10916143 | chr1:227427047 | A>T | SNV | Intergenic | AD |
rs1050492 | chr1:226632799 | G>A | SNV | ITPKB : 3 Prime UTR Variant | AD |
rs3219123 | chr1:226367647 | G>A / G>T | SNV | PARP1 : Intron Variant | ND |
rs3914465 | chr2:226310193 | A>G | SNV | Intergenic | AD |
rs4510219 | chr2:226284006 | A>C | SNV | Intergenic | AD |
rs964818 | chr2:226267064 | C>A | SNV | Intergenic | AD |
rs10198241 | chr2:226115660 | T>C | SNV | Intergenic | AD |
rs6664668 | chr1:226068253 | G>A | SNV | H3F3A : Intron Variant | ND |
rs7595617 | chr2:225650982 | A>G | SNV | NYAP2 : Intron Variant | AD |
rs1993323 | chr2:225591745 | C>A | SNV | NYAP2 : Intron Variant | AD |
rs3795443 | chr1:225487301 | A>G | SNV | ENAH : 3 Prime UTR Variant | ND |
rs10799590 | chr1:224634780 | G>A | SNV | CNIH3 : Intron Variant | OD |
rs851171 | chr1:223175678 | G>A | SNV | Intergenic | AD |
rs2936032 | chr1:222578449 | C>T | SNV | TAF1A : Intron Variant | AD |
rs11118748 | chr1:221541794 | C>T | SNV | Intergenic | ND |
rs11118607 | chr1:220811022 | C>T | SNV | MARC1 : Intron Variant | AD |
rs11118597 | chr1:220763226 | G>A | SNV | MARC2 : Intron Variant | AD |
rs3795536 | chr1:220762635 | G>A | SNV | MARC2 : Intron Variant | AD |
rs10779415 | chr1:220762466 | C>T | SNV | MARC2 : Intron Variant | AD |
rs6659246 | chr1:220757885 | C>A | SNV | MARC2 : Intron Variant | AD |
rs7530302 | chr1:220491610 | G>A | SNV | LOC105372928 : Intron Variant | ND |
rs7553380 | chr1:220452744 | A>G / A>T | SNV | Intergenic | ND |
rs7512221 | chr1:220428281 | C>T | SNV | Intergenic | ND |
rs12129498 | chr1:219934575 | A>G | SNV | SLC30A10 : Intron Variant LOC107985281 : Intron Variant | ND |
rs9661984 | chr1:218909718 | T>G | SNV | Intergenic | AD |
rs1001098 | chr2:217997518 | C>T | SNV | Intergenic | AD |
rs12759918 | chr1:217847795 | C>T | SNV | SPATA17 : Intron Variant | AD |
rs1567449 | chr1:217845614 | C>T | SNV | SPATA17 : Intron Variant | AD |
rs1549738 | chr2:217253999 | G>A | SNV | Intergenic | ND |
rs950614 | chr1:217191283 | G>A | SNV | LOC105372920 : 2KB Upstream Variant | AD |
rs11572505 | chr1:216920702 | T>C | SNV | ESRRG : Intron Variant | AD |
rs1436899 | chr1:216884140 | A>G | SNV | ESRRG : Intron Variant | ND |
rs7421283 | chr2:216776095 | C>T | SNV | LOC101928278 : Intron Variant | AD |
rs72737330 | chr1:216600151 | T>C | SNV | ESRRG : Intron Variant | AD |
rs7553212 | chr1:216565446 | A>G / A>T | SNV | ESRRG : Intron Variant | AD |
rs705648 | chr2:216069069 | C>T | SNV | PECR : Intron Variant | AD |
rs7590720 | chr2:216033935 | G>A | SNV | PECR : Intron Variant | AD |
rs1344694 | chr2:216028914 | T>G | SNV | PECR : 500B Downstream Variant | AD |
rs12126638 | chr1:216002354 | T>C | SNV | USH2A : Intron Variant | ND |
rs11120594 | chr1:215665748 | G>A | SNV | USH2A : Intron Variant | AD |
rs2677112 | chr1:215651825 | T>G | SNV | USH2A : Intron Variant | AD |
rs1911546 | chr1:215475754 | C>T | SNV | Intergenic | AD |
rs7594021 | chr2:214976105 | A>G | SNV | ABCA12 : Intron Variant | AD |
rs3795857 | chr2:214969952 | A>G / A>T | SNV | ABCA12 : Intron Variant | AD |
rs1464678 | chr2:214969742 | A>G | SNV | ABCA12 : Intron Variant | AD |
rs6756540 | chr2:214968898 | G>T | SNV | ABCA12 : Intron Variant | AD |
rs4673925 | chr2:214968691 | A>G | SNV | ABCA12 : Intron Variant | AD |
rs7534785 | chr1:214929079 | G>A | SNV | Intergenic | AD |
rs9288497 | chr2:214505328 | A>G | SNV | VWC2L : Intron Variant | AD |
rs4629153 | chr2:214492214 | C>T | SNV | VWC2L : Intron Variant | AD |
rs13425618 | chr2:214485443 | A>G | SNV | VWC2L : Intron Variant | AD |
rs6665548 | chr1:214243481 | A>G | SNV | Intergenic | AD |
rs1440620 | chr1:214088007 | T>C | SNV | LOC105372911 : Intron Variant | AD |
rs7597928 | chr2:213727658 | A>G | SNV | SPAG16 : Intron Variant | AD |
rs11120170 | chr1:213605853 | G>A | SNV | LOC105372912 : Intron Variant | AD |
rs16849209 | chr2:212746497 | G>T | SNV | Intergenic | AD |
rs675065 | chr1:212461241 | A>G | SNV | Intergenic | AD |
rs6711080 | chr2:212452605 | C>T | SNV | ERBB4 : Intron Variant | ND |
rs483954 | chr1:212446872 | A>G | SNV | NENF : 500B Downstream Variant | AD |
rs4804 | chr1:212445997 | T>C | SNV | NENF : Synonymous Variant | AD |
rs583058 | chr1:212437413 | T>C | SNV | NENF : Intron Variant | AD |
rs612414 | chr1:212428834 | G>A / G>T | SNV | Intergenic | AD |
rs6435678 | chr2:211845743 | G>C | SNV | ERBB4 : Intron Variant | ND |
rs11885579 | chr2:211566804 | A>G | SNV | ERBB4 : Intron Variant | AD |
rs13421680 | chr2:211551304 | A>G | SNV | ERBB4 : Intron Variant | AD |
rs6540681 | chr1:211320231 | A>G | SNV | Intergenic | AD |
rs1501551 | chr1:211003580 | C>T | SNV | KCNH1 : Intron Variant | AD |
rs1501558 | chr1:210953065 | G>A | SNV | KCNH1 : Intron Variant | AD |
rs12030256 | chr1:209030521 | T>C | SNV | LOC107985255 : Intron Variant | AD |
rs4844438 | chr1:208741511 | A>G | SNV | Intergenic | AD |
rs7591784 | chr2:207637006 | A>G | SNV | Intergenic | OD |
rs2709386 | chr2:207632310 | G>A | SNV | Intergenic | OD |
rs2952768 | chr2:207629510 | T>C | SNV | Intergenic | OD |
rs2254137 | chr2:207579304 | C>A | SNV | CREB1 : Intron Variant | OD |
rs12088135 | chr1:207079566 | C>T | SNV | PFKFB2 : 3 Prime UTR Variant | AD |
rs4845133 | chr1:206741989 | C>G | SNV | Intergenic | AD |
rs6677934 | chr1:206615113 | A>G | SNV | Intergenic | AD |
rs3755233 | chr2:205775107 | G>A | SNV | NRP2 : Intron Variant | ND |
rs7515820 | chr1:205584967 | A>C | SNV | MFSD4A : Synonymous Variant | AD |
rs11888554 | chr2:205231812 | C>A / C>T | SNV | PARD3B : Intron Variant | ND |
rs849118 | chr2:205160450 | G>A | SNV | PARD3B : Intron Variant | AD |
rs2082622 | chr2:205039410 | C>G | SNV | PARD3B : Intron Variant | ND |
rs7589114 | chr2:204911060 | C>T | SNV | PARD3B : Intron Variant | AD |
rs11801229 | chr1:204645347 | A>G | SNV | LRRN2 : Intron Variant | AD |
rs2137255 | chr1:204457245 | C>T | SNV | PIK3C2B : Intron Variant | AD |
rs4951373 | chr1:204423129 | G>A | SNV | PIK3C2B : Non Coding Transcript Variant | AD |
rs17478537 | chr2:203594456 | T>C | SNV | Intergenic | AD |
rs10800913 | chr1:203346765 | G>A | SNV | FMOD : Intron Variant | AD |
rs2117266 | chr2:203195425 | G>T | SNV | NBEAL1 : Intron Variant | AD |
rs10182274 | chr2:203186286 | G>A / G>T | SNV | NBEAL1 : Intron Variant | AD |
rs1038984 | chr1:203089714 | G>A | SNV | Intergenic | AD |
rs58592594 | chr1:203089348 | C>T | SNV | Intergenic | AD |
rs11685819 | chr2:202764034 | G>A | SNV | FAM117B : Intron Variant | AD |
rs2351117 | chr2:202762689 | C>T | SNV | FAM117B : Intron Variant | AD |
rs2351116 | chr2:202762588 | G>A | SNV | FAM117B : Intron Variant | AD |
rs6435163 | chr2:202744019 | T>C | SNV | FAM117B : Intron Variant | AD |
rs7581854 | chr2:202742031 | T>C | SNV | FAM117B : Intron Variant | AD |
rs7602496 | chr2:202737484 | C>A / C>T | SNV | FAM117B : Intron Variant | AD |
rs7571219 | chr2:202718531 | G>A | SNV | FAM117B : Intron Variant | AD |
rs6709463 | chr2:202680475 | C>T | SNV | FAM117B : Intron Variant | AD |
rs28760505 | chr2:202671092 | C>T | SNV | FAM117B : Intron Variant | AD |
rs13432396 | chr2:202604865 | C>A | SNV | Intergenic | AD |
rs116439821 | chr1:202215693 | C>T | SNV | LGR6 : Intron Variant | CD |
rs17435204 | chr1:202137868 | T>A / T>C | SNV | ARL8A : Intron Variant | ND |
rs7566288 | chr2:202064217 | G>T | SNV | Intergenic | AD |
rs2908763 | chr2:201503860 | T>C / T>G | SNV | ALS2CR11 : Intron Variant | AD |
rs1558637 | chr2:201398651 | G>A / G>T | SNV | TRAK2 : Intron Variant | AD |
rs2244438 | chr2:201387816 | G>A / G>T | SNV | TRAK2 : Missense Variant | AD |
rs2799686 | chr1:201378187 | A>G | SNV | TNNT2 : 2KB Upstream Variant | AD |
rs10202963 | chr2:201377184 | T>G | SNV | TRAK2 : 500B Downstream Variant | AD |
rs2275863 | chr1:201359696 | G>A / G>T | SNV | TNNT2 : Intron Variant | AD |
rs9288318 | chr2:201331340 | C>A | SNV | ALS2CR12 : Intron Variant | AD |
rs7563911 | chr2:200711561 | A>C / A>G | SNV | AOX3P-AOX2P : Intron Variant | AD |
rs2253612 | chr2:200703710 | C>T | SNV | AOX3P-AOX2P : Intron Variant | AD |
rs2241080 | chr2:200662516 | G>A / G>T | SNV | AOX1 : Intron Variant | AD |
rs3815502 | chr2:200661197 | C>A / C>G | SNV | AOX1 : Intron Variant | AD |
rs2028201 | chr2:200438287 | G>T | SNV | SPATS2L : Intron Variant LOC101927741 : Intron Variant | AD |
rs1060061 | chr1:200174314 | T>C | SNV | NR5A2 : 3 Prime UTR Variant | ND |
rs10189905 | chr2:198814386 | T>G | SNV | Intergenic | ND |
rs16843093 | chr1:198447545 | A>G | SNV | Intergenic | ND |
rs16843001 | chr1:198404196 | T>C | SNV | Intergenic | ND |
rs16842754 | chr1:198308005 | C>A | SNV | NEK7 : Intron Variant | ND |
rs12407433 | chr1:198305778 | A>T | SNV | NEK7 : Intron Variant | ND |
rs10494769 | chr1:198305231 | A>G | SNV | NEK7 : Intron Variant | ND |
rs16842733 | chr1:198304970 | A>G | SNV | NEK7 : Intron Variant | ND |
rs16842730 | chr1:198304759 | G>A | SNV | NEK7 : Intron Variant | ND |
rs1475423 | chr1:198254360 | A>T | SNV | NEK7 : Intron Variant | ND |
rs10494765 | chr1:198245912 | T>G | SNV | NEK7 : Intron Variant | ND |
rs10180112 | chr2:198118134 | C>G | SNV | PLCL1 : Intron Variant | AD |
rs9973400 | chr2:198076854 | T>C | SNV | PLCL1 : Intron Variant | AD |
rs1866666 | chr2:198075883 | T>C / T>G | SNV | PLCL1 : Intron Variant | AD |
rs11690205 | chr2:198069224 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs11690149 | chr2:198069080 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs7587251 | chr2:198065473 | T>G | SNV | PLCL1 : Intron Variant | AD |
rs7572733 | chr2:198065082 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs35062652 | chr2:198063203 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs2117339 | chr2:198051010 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs10497813 | chr2:198049348 | G>T | SNV | PLCL1 : Intron Variant | AD |
rs6732340 | chr2:198048228 | C>G | SNV | PLCL1 : Intron Variant | AD |
rs67031482 | chr2:198046442 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs745899 | chr2:198043316 | A>T | SNV | PLCL1 : Intron Variant | AD |
rs9712275 | chr2:198042419 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs10206714 | chr2:198041757 | C>A / C>T | SNV | PLCL1 : Intron Variant | AD |
rs12329164 | chr2:198040500 | C>A / C>G | SNV | PLCL1 : Intron Variant | AD |
rs2196174 | chr2:198040448 | A>G | SNV | PLCL1 : Intron Variant | AD |
rs2196175 | chr2:198040349 | T>A | SNV | PLCL1 : Intron Variant | AD |
rs1371664 | chr2:198039741 | T>A | SNV | PLCL1 : Intron Variant | AD |
rs10497811 | chr2:198038185 | A>C | SNV | PLCL1 : Intron Variant | AD |
rs962210 | chr2:198037506 | A>T | SNV | PLCL1 : Intron Variant | AD |
rs1579695 | chr2:198035639 | G>A | SNV | PLCL1 : Intron Variant | AD |
rs1583792 | chr2:198035564 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs11889326 | chr2:198034551 | A>C | SNV | PLCL1 : Intron Variant | AD |
rs1541953 | chr2:198033620 | A>T | SNV | PLCL1 : Intron Variant | AD |
rs6738825 | chr2:198032171 | A>G | SNV | PLCL1 : Intron Variant | AD |
rs10166845 | chr2:198031347 | A>G | SNV | PLCL1 : Intron Variant | AD |
rs10184227 | chr2:198029581 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs10196612 | chr2:198029415 | T>C | SNV | PLCL1 : Intron Variant | AD |
rs1595823 | chr2:198027075 | C>T | SNV | PLCL1 : Intron Variant | AD |
rs2196172 | chr2:198025169 | T>G | SNV | PLCL1 : Intron Variant | AD |
rs2196171 | chr2:198025083 | T>A / T>G | SNV | PLCL1 : Intron Variant | AD |
rs1978888 | chr2:198024521 | T>C | SNV | PLCL1 : Intron Variant | AD |
rs2139049 | chr2:198022936 | G>A | SNV | PLCL1 : Intron Variant | AD |
rs11683222 | chr2:198019304 | C>G | SNV | PLCL1 : Intron Variant | AD |
rs34692727 | chr2:198018789 | C>G / C>T | SNV | PLCL1 : Intron Variant | AD |
rs11681663 | chr2:198018228 | G>A | SNV | PLCL1 : Intron Variant | AD |
rs1025549 | chr2:198016459 | G>A | SNV | PLCL1 : Intron Variant | AD |
rs10922323 | chr1:197893191 | T>C | SNV | Intergenic | AD |
rs10801629 | chr1:197875237 | C>T | SNV | Intergenic | AD |
rs58335266 | chr2:197505616 | G>A | SNV | HSPE1-MOB4 : Intron Variant | AD |
rs55702914 | chr2:197349672 | C>G | SNV | Intergenic | AD |
rs1896857 | chr2:197299806 | A>G | SNV | ANKRD44 : Intron Variant ANKRD44-IT1 : Intron Variant | AD |
rs843511 | chr3:196687288 | C>T | SNV | Intergenic | AD |
rs10197202 | chr2:196658242 | G>A | SNV | CCDC150 : Intron Variant | AD |
rs12036795 | chr1:196120688 | A>C | SNV | Intergenic | AD |
rs11579497 | chr1:196092581 | G>A | SNV | Intergenic | AD |
rs6677435 | chr1:195821528 | G>A | SNV | Intergenic | CD |
rs6743998 | chr2:195811765 | T>C | SNV | DNAH7 : Intron Variant | AD |
rs6434799 | chr2:195800359 | C>T | SNV | DNAH7 : Intron Variant LOC105373819 : Intron Variant | AD |
rs6756374 | chr2:195722946 | C>A | SNV | SLC39A10 : Intron Variant | AD |
rs6706771 | chr2:195700517 | G>A / G>T | SNV | SLC39A10 : Intron Variant | AD |
rs1561451 | chr2:195684712 | A>G | SNV | SLC39A10 : Intron Variant | AD |
rs10178320 | chr2:195677278 | T>C | SNV | SLC39A10 : Intron Variant | AD |
rs1866452 | chr2:195671781 | A>G | SNV | SLC39A10 : Intron Variant | AD |
rs7424415 | chr2:195671426 | T>C | SNV | SLC39A10 : Intron Variant | AD |
rs11682521 | chr2:195652785 | G>A | SNV | SLC39A10 : Intron Variant | AD |
rs10460389 | chr2:195641240 | C>A | SNV | SLC39A10 : Intron Variant | AD |
rs7627066 | chr3:194512024 | T>G | SNV | Intergenic | AD |
rs1572840 | chr3:194398854 | G>A | SNV | GP5 : Intron Variant | AD |
rs9869202 | chr3:192907401 | C>A / C>T | SNV | MB21D2 : Intron Variant | AD |
rs7643379 | chr3:192901594 | A>G | SNV | MB21D2 : Intron Variant | AD |
rs3952738 | chr3:192896694 | T>C | SNV | MB21D2 : Intron Variant | AD |
rs4455277 | chr3:192896519 | T>C | SNV | MB21D2 : Intron Variant | AD |
rs2062832 | chr3:192623262 | T>C | SNV | FGF12 : Intron Variant | AD |
rs1922910 | chr3:192621072 | A>G | SNV | FGF12 : Intron Variant | AD |
rs6779599 | chr3:192130010 | C>A | SNV | Intergenic | AD |
rs16833847 | chr1:191850751 | A>G | SNV | Intergenic | ND |
rs4592792 | chr2:191667291 | A>G | SNV | Intergenic | AD |
rs6690512 | chr1:191371813 | G>A | SNV | Intergenic | AD |
rs9864764 | chr3:190996798 | A>C | SNV | Intergenic | AD |
rs6778263 | chr3:190920044 | C>A | SNV | Intergenic | AD |
rs62184317 | chr2:189917038 | C>T | SNV | C2orf88 : Intron Variant LOC105373795 : Intron Variant | AD |
rs7563391 | chr2:189915077 | G>C | SNV | C2orf88 : Intron Variant LOC105373795 : Intron Variant | AD |
rs62184315 | chr2:189907219 | T>C | SNV | C2orf88 : Intron Variant LOC105373795 : Intron Variant | AD |
rs10188230 | chr2:189567887 | T>C | SNV | SLC40A1 : Intron Variant | AD |
rs11539983 | chr2:189560748 | T>C | SNV | SLC40A1 : 3 Prime UTR Variant | AD |
rs17271148 | chr2:189537496 | G>A | SNV | Intergenic | AD |
rs938413 | chr3:188646825 | C>T | SNV | LPP : Intron Variant | AD |
rs6807897 | chr3:188515616 | G>A | SNV | LPP : Intron Variant | ND |
rs284046 | chr1:188456602 | A>C | SNV | Intergenic | ND |
rs11930915 | chr4:188326619 | G>A / G>T | SNV | Intergenic | ND |
rs7683009 | chr4:187776941 | C>T | SNV | Intergenic | AD |
rs1938512 | chr1:187453740 | C>A / C>G | SNV | LINC01037 : Intron Variant | AD |
rs3105782 | chr3:187253508 | A>G | SNV | MASP1 : Intron Variant | ND |
rs1474797 | chr1:186998061 | A>G | SNV | Intergenic | OD |
rs761516 | chr1:186992194 | T>C / T>G | SNV | Intergenic | AD |
rs2205953 | chr1:186723430 | T>C | SNV | Intergenic | AD |
rs6553017 | chr4:186660322 | G>T | SNV | FAT1 : Intron Variant | ND |
rs2280390 | chr3:186576031 | T>G | SNV | DNAJB11 : Intron Variant | AD |
rs1868152 | chr3:186502274 | A>G / A>T | SNV | Intergenic | AD | ND |
rs11918665 | chr3:186495995 | A>G | SNV | Intergenic | AD | ND |
rs10497668 | chr2:186349003 | T>C | SNV | Intergenic | AD |
rs16827526 | chr2:186176102 | T>G | SNV | Intergenic | AD |
rs964744 | chr2:186017422 | C>T | SNV | Intergenic | AD |
rs9864104 | chr3:185639743 | C>T | SNV | Intergenic | AD |
rs6818704 | chr4:185125319 | A>G | SNV | Intergenic | AD |
rs10009538 | chr4:184971361 | C>A / C>T | SNV | Intergenic | AD |
rs9883278 | chr3:184758045 | G>A | SNV | LOC101928992 : Non Coding Transcript Variant | AD |
rs7698703 | chr4:184539168 | G>A | SNV | LOC105377585 : 2KB Upstream Variant | AD |
rs2001270 | chr1:184524750 | A>G | SNV | C1orf21 : Intron Variant | AD |
rs3930234 | chr3:184498342 | T>C | SNV | LOC105374252 : Intron Variant | AD |
rs1882331 | chr4:184202613 | T>C | SNV | ENPP6 : Intron Variant | AD |
rs6552767 | chr4:184188841 | G>A | SNV | ENPP6 : Intron Variant | AD |
rs13262 | chr3:184183601 | T>C | SNV | AP2M1 : Synonymous Variant | AD |
rs11132226 | chr4:184144142 | G>A | SNV | ENPP6 : Intron Variant | ND |
rs1000002 | chr3:183917980 | C>T | SNV | Intergenic | AD |
rs6807489 | chr3:183676674 | A>G | SNV | KLHL24 : Intron Variant | AD |
rs2368446 | chr2:183543235 | T>C | SNV | Intergenic | AD |
rs12635655 | chr3:183378194 | C>A / C>T | SNV | MCF2L2 : Intron Variant | AD |
rs16860582 | chr1:183221316 | T>C | SNV | LAMC2 : Intron Variant | AD |
rs1377943 | chr4:183008428 | C>T | SNV | Intergenic | AD |
rs10797794 | chr1:182888873 | G>A | SNV | Intergenic | CD |
rs4384980 | chr3:182741281 | A>C | SNV | Intergenic | AD |
rs12564594 | chr1:182147233 | A>G | SNV | ZNF648 : Intron Variant | AD |
rs16822370 | chr2:182041984 | G>T | SNV | PPP1R1C : Intron Variant | AD |
rs6552517 | chr4:181655433 | C>T | SNV | TENM3 : Intron Variant | AD |
rs3789373 | chr1:180804994 | C>T | SNV | XPR1 : Intron Variant | AD |
rs2387207 | chr5:180684144 | C>T | SNV | LOC105377765 : Non Coding Transcript Variant | AD |
rs6836406 | chr4:179981761 | A>G | SNV | LOC105377564 : Intron Variant | AD |
rs17769849 | chr4:179978312 | C>T | SNV | LOC105377564 : Intron Variant | AD |
rs9823402 | chr3:179851760 | G>A | SNV | PEX5L : Intron Variant | AD |
rs7640024 | chr3:179851152 | G>A | SNV | PEX5L : Intron Variant | AD |
rs6443673 | chr3:179848495 | C>T | SNV | PEX5L : Intron Variant | AD |
rs16854429 | chr1:179640454 | G>C / G>T | SNV | TDRD5 : Intron Variant | AD |
rs2274626 | chr1:179552797 | G>T | SNV | AXDND1 : Intron VariantNPHS2 : Intron Variant | AD |
rs1410587 | chr1:179546937 | C>G / C>T | SNV | AXDND1 : Intron Variant | AD |
rs10017041 | chr4:179545156 | T>C | SNV | Intergenic | AD |
rs166031 | chr5:179293967 | A>G | SNV | ADAMTS2 : Intron Variant | AD |
rs17592582 | chr3:179192562 | T>C | SNV | PIK3CA : Intron Variant | AD |
rs2645339 | chr5:178989062 | G>A | SNV | GRM6 : Synonymous Variant | ND |
rs17355446 | chr2:178724514 | G>A | SNV | TTN : Missense Variant | ND |
rs10913569 | chr1:178548873 | A>G | SNV | C1orf220 : Non Coding Transcript Variant | AD |
rs4233175 | chr1:178548456 | A>G | SNV | C1orf220 : Non Coding Transcript Variant | AD |
rs2666055 | chr4:178423266 | G>A | SNV | Intergenic | AD |
rs1567479 | chr4:178386739 | G>A | SNV | Intergenic | AD |
rs2705988 | chr4:178369239 | G>A | SNV | Intergenic | AD |
rs2705962 | chr4:178358811 | A>G | SNV | Intergenic | AD |
rs993598 | chr2:178317968 | G>A | SNV | OSBPL6 : Intron Variant | AD |
rs2913848 | chr5:178257021 | C>T | SNV | COL23A1 : Intron Variant | AD |
rs2961663 | chr5:178186543 | C>G / C>T | SNV | GMCL1P1 : Non Coding Transcript Variant | AD |
rs7715618 | chr5:178185633 | A>C | SNV | GMCL1P1 : Non Coding Transcript Variant | AD |
rs7719717 | chr5:178185292 | T>G | SNV | GMCL1P1 : Non Coding Transcript Variant | AD |
rs7380658 | chr5:178185033 | G>T | SNV | GMCL1P1 : Non Coding Transcript Variant | AD |
rs9329136 | chr5:178184647 | G>A | SNV | GMCL1P1 : Non Coding Transcript Variant | AD |
rs553372 | chr4:178125465 | G>A | SNV | Intergenic | AD |
rs12517913 | chr5:178078794 | C>T | SNV | Intergenic | OD |
rs2117740 | chr2:178025602 | A>G | SNV | PDE11A : Intron Variant | AD |
rs6443523 | chr3:177987280 | G>A | SNV | Intergenic | ND |
rs1353899 | chr3:177511191 | T>A / T>G | SNV | LINC00578 : Intron Variant | AD |
rs59539624 | chr3:177509729 | G>C / G>T | SNV | LINC00578 : Intron Variant | AD |
rs7615202 | chr3:177505279 | T>C | SNV | LINC00578 : Intron Variant | AD |
rs1392219 | chr3:177504641 | C>T | SNV | LINC00578 : Intron Variant | AD |
rs12026256 | chr1:177464440 | A>G | SNV | Intergenic | AD |
rs9850957 | chr3:177395268 | C>T | SNV | Intergenic | AD |
rs7632766 | chr3:177150265 | T>C | SNV | TBL1XR1 : Intron Variant | AD |
rs1209035 | chr3:177110139 | T>C | SNV | TBL1XR1 : Intron Variant | AD |
rs4894243 | chr2:177097413 | C>T | SNV | LOC105373760 : Intron Variant | AD |
rs1201284 | chr3:177089526 | G>A / G>T | SNV | TBL1XR1 : Intron Variant | AD |
rs12135256 | chr1:177006309 | C>G | SNV | ASTN1 : Intron Variant | AD |
rs13170785 | chr5:176368663 | G>A | SNV | ARL10 : Intron Variant | AD |
rs10063877 | chr5:176357917 | T>C | SNV | KIAA1191 : Intron Variant | AD |
rs11134974 | chr5:176354956 | C>T | SNV | KIAA1191 : Intron Variant | AD |
rs3749804 | chr5:176349152 | A>G | SNV | KIAA1191 : Intron Variant | AD |
rs11134973 | chr5:176343419 | C>T | SNV | SIMC1 : Intron Variant | AD |
rs11134972 | chr5:176343418 | G>A | SNV | SIMC1 : Intron Variant | AD |
rs13169783 | chr5:176337365 | T>C | SNV | SIMC1 : Intron Variant | AD |
rs9835842 | chr3:176313899 | A>G | SNV | Intergenic | AD |
rs2166512 | chr2:176206453 | T>C | SNV | Intergenic | AD |
rs1026028 | chr2:176206028 | C>A | SNV | Intergenic | AD |
rs718907 | chr5:175716629 | C>A | SNV | Intergenic | AD |
rs58398985 | chr3:175318979-175318983 | dupT | Indel | NAALADL2 : Intron Variant | AD |
rs10489326 | chr1:175165541 | A>G | SNV | KIAA0040 : Intron Variant | AD |
rs1894709 | chr1:175163235 | G>T | SNV | KIAA0040 : Intron Variant | AD | ND |
rs1057239 | chr1:175161068 | G>A | SNV | KIAA0040 : 5 Prime UTR Variant | AD | ND |
rs4650716 | chr1:175159575 | C>A | SNV | KIAA0040 : 3 Prime UTR Variant | AD |
rs1057302 | chr1:175157287 | A>G | SNV | KIAA0040 : 3 Prime UTR Variant | AD |
rs6425323 | chr1:175155900 | C>T | SNV | Intergenic | AD |
rs6701037 | chr1:175150943 | A>C | SNV | Intergenic | AD |
rs13388308 | chr2:175141299 | C>T | SNV | ATF2 : Intron Variant | AD |
rs2157588 | chr1:175138690 | C>T | SNV | TNN : Intron Variant | AD |
rs12094153 | chr1:175124889 | G>A | SNV | TNN : Intron Variant | AD |
rs1153676 | chr2:175116266 | C>A | SNV | ATF2 : Intron Variant | AD |
rs2072538 | chr2:175097936 | C>T | SNV | ATF2 : Intron Variant | AD |
rs35522805 | chr2:175087402 | G>A | SNV | ATF2 : Intron Variant | AD |
rs212349 | chr2:175079670 | T>C | SNV | ATF2 : Intron Variant | AD |
rs10513729 | chr3:174963457 | T>G | SNV | NAALADL2 : Intron Variant | AD |
rs3753563 | chr1:174954209 | T>C | SNV | RABGAP1L : Intron Variant LOC101928696 : Non Coding Transcript Variant | AD |
rs4868468 | chr5:174952561 | G>A | SNV | FLJ16171 : Intron Variant | AD |
rs17064145 | chr5:174948706 | C>A | SNV | FLJ16171 : Intron Variant | AD |
rs6824735 | chr4:174819418 | T>C | SNV | GLRA3 : Intron Variant | AD |
rs55768019 | chr4:174106365 | A>G | SNV | LOC101928509 : Intron Variant | AD |
rs10497422 | chr2:173988057 | G>T | SNV | Intergenic | AD |
rs11944332 | chr4:173633681 | A>G | SNV | Intergenic | CD |
rs4129566 | chr4:173626006 | T>C | SNV | Intergenic | CD |
rs4639045 | chr4:173600164 | T>C | SNV | Intergenic | CD |
rs1363605 | chr5:173590084 | C>T | SNV | Intergenic | AD |
rs746215 | chr5:173584350 | T>C | SNV | LOC285593 : Non Coding Transcript Variant LOC105377735 : Non Coding Transcript Variant | AD |
rs10077254 | chr5:173579444 | C>T | SNV | LOC285593 : 2KB Upstream Variant | AD |
rs844656 | chr1:173266696 | T>G | SNV | TNFSF4 : Intron Variant LOC100506023 : Intron Variant | AD |
rs6761224 | chr2:173261232 | T>C | SNV | ZAK : Intron Variant MLK7-AS1 : Intron Variant | AD |
rs13176814 | chr5:172864246 | A>G | SNV | ERGIC1 : Intron Variant | AD |
rs74426112 | chr2:172713180 | C>T | SNV | Intergenic | CD |
rs2859242 | chr1:172655724 | C>T | SNV | Intergenic | AD |
rs1541918 | chr5:172544483 | C>A | SNV | Intergenic | AD |
rs2041692 | chr3:172497847 | T>C | SNV | Intergenic | AD |
rs6698987 | chr1:172399827 | T>C | SNV | DNM3 : Intron Variant LOC102724528 : Non Coding Transcript Variant | AD |
rs788160 | chr2:172081587 | T>A / T>G | SNV | METAP1D : Non Coding Transcript Variant | AD |
rs17427473 | chr2:171719501 | A>G | SNV | DYNC1I2 : Intron Variant | ND |
rs12634193 | chr3:171462896 | T>C | SNV | LOC102724479 : Intron Variant | ND |
rs11926949 | chr3:171377305 | T>C / T>G | SNV | TNIK : Intron Variant | AD |
rs6830239 | chr4:171226645 | G>A | SNV | Intergenic | AD |
rs16859177 | chr2:171150066 | C>T | SNV | TLK1 : Intron Variant | AD |
rs4955765 | chr3:171113283 | G>A | SNV | TNIK : Intron Variant LOC105374216 : Intron Variant | AD |
rs7051320 | chr1:171110559 | C>T | SNV | FMO3 : Intron Variant | AD |
rs7701805 | chr5:170942597 | T>A / T>C | SNV | RANBP17 : Intron Variant | ND |
rs3791853 | chr2:170838560 | A>G | SNV | GAD1 : Intron Variant | AD |
rs1808374 | chr5:170826977 | C>T | SNV | Intergenic | AD |
rs11134638 | chr5:170580499 | A>G | SNV | KCNIP1 : Intron Variant | AD |
rs888936 | chr5:170496899 | C>T | SNV | KCNIP1 : Intron Variant | AD |
rs1412787 | chr1:170239583 | C>T | SNV | LOC105371609 : Non Coding Transcript Variant | AD |
rs10158534 | chr1:170203276 | T>G | SNV | LOC105371609 : Intron Variant | AD |
rs9348260 | chr6:170200899 | G>A | SNV | Intergenic | AD |
rs1381471 | chr2:170097896 | T>C | SNV | Intergenic | AD |
rs2466990 | chr4:170072620 | A>G | SNV | AADAT : Intron Variant | AD |
rs1316638 | chr5:170050007 | T>C | SNV | DOCK2 : Intron Variant | AD |
rs3769769 | chr2:169819255 | C>T | SNV | METTL5 : Intron Variant | AD |
rs5353 | chr1:169733833 | T>C | SNV | SELE : Intron Variant | AD |
rs932307 | chr1:169733564 | G>A | SNV | SELE : Intron Variant | AD |
rs3917419 | chr1:169730678 | G>A | SNV | SELE : Intron Variant | AD |
rs9478099 | chr6:169730151 | G>C | SNV | TCTE3 : Intron Variant | AD |
rs1076637 | chr1:169728303 | C>T | SNV | SELE : Intron Variant | AD |
rs5359 | chr1:169723381 | T>C | SNV | SELE : 3 Prime UTR Variant | AD |
rs4786 | chr1:169722991 | T>C | SNV | SELE : 3 Prime UTR Variant | AD |
rs3917449 | chr1:169722078 | G>A | SNV | Intergenic | AD |
rs4656703 | chr1:169718994 | A>C | SNV | Intergenic | AD |
rs2205849 | chr1:169712216 | T>C | SNV | SELL : 2KB Upstream Variant | AD |
rs4987285 | chr1:169708883 | T>C | SNV | SELL : Intron Variant | AD |
rs1051091 | chr1:169708568 | A>G | SNV | SELL : Synonymous Variant | AD |
rs2205847 | chr1:169707082 | G>T | SNV | SELL : Intron Variant | AD |
rs2229569 | chr1:169704697 | G>A / G>T | SNV | SELL : Missense Variant | AD |
rs4987314 | chr1:169703202 | C>G / C>T | SNV | SELL : Intron Variant | AD |
rs2306559 | chr5:169702418 | A>G | SNV | DOCK2 : Synonymous Variant | AD |
rs964555 | chr1:169701947 | A>C | SNV | SELL : Intron Variant | AD |
rs7349274 | chr2:169529784 | G>A | SNV | FASTKD1 : Non Coding Transcript Variant | AD |
rs368028 | chr6:169411199 | C>T | SNV | Intergenic | AD |
rs1420469 | chr3:169024673 | T>C | SNV | Intergenic | AD |
rs6831359 | chr4:168751479 | A>G | SNV | PALLD : Intron Variant | AD |
rs6777018 | chr3:168448398 | A>G | SNV | EGFEM1P : Intron Variant | AD |
rs2076663 | chr6:167974511 | C>T | SNV | Intergenic | AD |
rs1363204 | chr5:167893080 | T>A | SNV | TENM2 : Intron Variant | ND |
rs1897339 | chr2:167551928 | T>G | SNV | B3GALT1 : Intron Variant | AD |
rs1229430 | chr1:167544181 | C>T | SNV | CREG1 : Intron Variant | AD |
rs4955672 | chr3:167457459 | C>G | SNV | SERPINI2 : Intron Variant | AD |
rs13074970 | chr3:167402157 | C>T | SNV | LINC01327 : Intron Variant | AD |
rs1053407 | chr1:166913500 | C>T | SNV | ILDR2 : 3 Prime UTR Variant | AD |
rs4656517 | chr1:166886822 | G>A | SNV | Intergenic | AD |
rs6935679 | chr6:166667229 | A>G | SNV | RPS6KA2 : Intron Variant | ND |
rs6536987 | chr4:166607472 | A>G | SNV | Intergenic | AD |
rs12506794 | chr4:166533135 | C>T | SNV | Intergenic | AD |
rs978230 | chr4:166500964 | C>T | SNV | Intergenic | AD |
rs526992 | chr3:166310918 | T>C | SNV | Intergenic | AD |
rs10041088 | chr5:165640813 | G>A | SNV | Intergenic | ND |
rs10211296 | chr2:165633833 | A>G | SNV | CSRNP3 : Intron Variant | AD |
rs1370687 | chr4:165469203 | C>T | SNV | CPE : Intron Variant | AD |
rs6536915 | chr4:165463215 | C>T | SNV | CPE : Intron Variant | AD |
rs9459418 | chr6:165454303 | C>A | SNV | PDE10A : Intron Variant | AD |
rs687415 | chr2:165447088 | C>T | SNV | Intergenic | AD |
rs220821 | chr6:165435750 | A>C | SNV | PDE10A : Intron Variant | AD |
rs729699 | chr4:165414029 | C>A / C>T | SNV | CPE : Intron Variant | AD |
rs17686882 | chr4:165401246 | G>A / G>T | SNV | CPE : Intron Variant | CD |
rs35355030 | chr4:165394348 | T>C | SNV | CPE : Intron Variant | CD |
rs4691188 | chr4:165391348 | C>T | SNV | CPE : Intron Variant | CD |
rs9631752 | chr4:165390534 | A>T | SNV | CPE : Intron Variant | CD |
rs12513327 | chr4:165224668 | G>A | SNV | KLHL2 : Intron Variant | ND |
rs2028891 | chr2:165211148 | T>G | SNV | SCN2A : Intron Variant | AD |
rs506879 | chr6:165167517 | C>A / C>T | SNV | Intergenic | AD |
rs11916446 | chr3:165118584 | G>T | SNV | Intergenic | AD |
rs1347992 | chr2:165105355 | T>C | SNV | SCN3A : Intron Variant | AD |
rs3816195 | chr2:165099998 | T>G | SNV | SCN3A : Intron Variant | AD |
rs2168784 | chr3:164872151 | C>T | SNV | Intergenic | AD |
rs56303997 | chr3:164871362 | G>A | SNV | Intergenic | AD |
rs9810313 | chr3:164870914 | G>T | SNV | Intergenic | AD |
rs6788557 | chr3:164870600 | C>G | SNV | Intergenic | AD |
rs6763281 | chr3:164870417 | G>T | SNV | Intergenic | AD |
rs6808582 | chr3:164869771 | G>A | SNV | Intergenic | AD |
rs7641732 | chr3:164869562 | A>T | SNV | Intergenic | AD |
rs9879548 | chr3:164869514 | G>T | SNV | Intergenic | AD |
rs5023277 | chr3:164868927 | C>G | SNV | Intergenic | AD |
rs6791103 | chr3:164867787 | A>C | SNV | Intergenic | AD |
rs7619524 | chr3:164862884 | C>T | SNV | Intergenic | AD |
rs9865078 | chr3:164861522 | G>A / G>C | SNV | Intergenic | AD |
rs4602392 | chr3:164860478 | C>T | SNV | Intergenic | AD |
rs9881091 | chr3:164855523 | T>G | SNV | Intergenic | AD |
rs7628882 | chr3:164853350 | G>A / G>T | SNV | Intergenic | AD |
rs9290244 | chr3:164850775 | T>G | SNV | Intergenic | AD |
rs9830200 | chr3:164849971 | G>A | SNV | Intergenic | AD |
rs9819217 | chr3:164847975 | C>T | SNV | Intergenic | AD |
rs9873722 | chr3:164845602 | A>G | SNV | Intergenic | AD |
rs9855885 | chr3:164845413 | T>C | SNV | Intergenic | AD |
rs7640074 | chr3:164844376 | C>G / C>T | SNV | Intergenic | AD |
rs7647704 | chr3:164842406 | T>A | SNV | Intergenic | AD |
rs7645282 | chr3:164842394 | A>G | SNV | Intergenic | AD |
rs28821642 | chr3:164841642 | C>T | SNV | Intergenic | AD |
rs9847462 | chr3:164840807 | A>G | SNV | Intergenic | AD |
rs4541411 | chr3:164840129 | T>C | SNV | Intergenic | AD |
rs9880338 | chr3:164839864 | G>A | SNV | Intergenic | AD |
rs9824625 | chr3:164839787 | T>C | SNV | Intergenic | AD |
rs9874932 | chr3:164838860 | G>A / G>T | SNV | Intergenic | AD |
rs7630142 | chr3:164837918 | A>G | SNV | Intergenic | AD |
rs9817317 | chr3:164837013 | G>A | SNV | Intergenic | AD |
rs9816120 | chr3:164836235 | G>T | SNV | Intergenic | AD |
rs9831395 | chr3:164835787 | T>C | SNV | Intergenic | AD |
rs9825394 | chr3:164834344 | T>C | SNV | Intergenic | AD |
rs7633723 | chr3:164833256 | T>C | SNV | LINC01324 : 2KB Upstream Variant | AD |
rs57369046 | chr3:164831898 | T>C | SNV | LINC01324 : 2KB Upstream Variant | AD |
rs9849299 | chr3:164828470 | G>A / G>T | SNV | LINC01324 : Intron Variant | AD |
rs9824015 | chr3:164825840 | A>G | SNV | LINC01324 : Intron Variant | AD |
rs9876205 | chr3:164824737 | T>C | SNV | LINC01324 : Intron Variant | AD |
rs10433463 | chr3:164822861 | G>A | SNV | LINC01324 : Intron Variant | AD |
rs9838822 | chr3:164817726 | T>C | SNV | LINC01324 : Intron Variant | AD |
rs10936425 | chr3:164816238 | A>G | SNV | LINC01324 : Intron Variant | AD |
rs9862987 | chr3:164813439 | A>C | SNV | LINC01324 : Intron Variant | AD |
rs10494422 | chr1:164811778 | A>C | SNV | PBX1 : Intron Variant | ND |
rs9875364 | chr3:164803065 | G>C | SNV | LINC01324 : Intron Variant | AD |
rs9871275 | chr3:164802995 | C>T | SNV | LINC01324 : Intron Variant | AD |
rs57350471 | chr3:164802975 | T>A | SNV | LINC01324 : Intron Variant | AD |
rs10494419 | chr1:164642664 | T>G | SNV | PBX1 : Intron Variant | AD |
rs4423615 | chr2:164581720 | G>A | SNV | GRB14 : Intron Variant | ND |
rs10800021 | chr1:164485412 | C>G | SNV | Intergenic | ND |
rs2027290 | chr1:164485313 | A>C | SNV | Intergenic | ND |
rs7517505 | chr1:164484136 | T>C | SNV | Intergenic | ND |
rs7550193 | chr1:164483505 | G>C | SNV | Intergenic | ND |
rs1417056 | chr6:164431199 | A>G | SNV | Intergenic | ND |
rs2964911 | chr5:164297275 | A>G | SNV | LOC105377703 : Intron Variant | ND |
rs395843 | chr6:164057884 | T>C | SNV | LOC105378102 : Intron Variant | AD |
rs1460673 | chr2:163745636 | A>G | SNV | Intergenic | AD |
rs1407662 | chr6:163670625 | A>G | SNV | LOC102724152 : Intron Variant LOC107986666 : 2KB Upstream Variant | AD |
rs3967768 | chr4:163268711 | G>A | SNV | Intergenic | ND |
rs12730805 | chr1:162903430 | C>A | SNV | Intergenic | AD |
rs312312 | chr5:162633359 | A>G | SNV | LOC105377698 : Intron Variant | AD |
rs172676 | chr5:162616844 | A>C / A>G / A>T | SNV | Intergenic | AD |
rs6681981 | chr1:162361831 | A>G | SNV | NOS1AP : Intron Variant | AD |
rs3788964 | chr2:162350970 | T>C | SNV | GCA : Intron Variant | ND |
rs4440177 | chr4:162321901 | G>A | SNV | Intergenic | ND | AD |
rs4709595 | chr6:162308349 | G>T | SNV | PARK2 : Intron Variant | ND |
rs4656355 | chr1:162154007 | A>G | SNV | NOS1AP : Intron Variant LOC105371475 : Intron Variant | AD |
rs1932933 | chr1:162148256 | T>C | SNV | NOS1AP : Intron Variant LOC105371475 : Intron Variant | AD |
rs2268888 | chr2:162028940 | C>T | SNV | DPP4 : Intron Variant | AD |
rs16846221 | chr2:161963710 | G>T | SNV | SLC4A10 : Intron Variant | AD |
rs17536732 | chr4:161903214 | G>T | SNV | FSTL5 : Intron Variant | AD |
rs115460205 | chr4:161890417 | C>T | SNV | FSTL5 : Intron Variant | AD |
rs1440588 | chr4:161842862 | A>G | SNV | FSTL5 : Intron Variant | AD |
rs1954174 | chr1:161708017 | C>T | SNV | FCRLA : Intron Variant | AD |
rs17479823 | chr3:161511426 | C>G / C>T | SNV | Intergenic | AD |
rs7644500 | chr3:161506750 | G>A | SNV | Intergenic | ND |
rs16892573 | chr6:161475487 | G>A / G>C | SNV | PARK2 : Intron Variant LOC105378098 : Intron Variant | ND |
rs12191615 | chr6:161144126 | T>C | SNV | AGPAT4 : Intron Variant | AD |
rs9458121 | chr6:161101446 | A>G | SNV | MAP3K4 : Intron Variant | AD |
rs9355870 | chr6:161074626 | A>G | SNV | MAP3K4 : Intron Variant | AD |
rs12110787 | chr6:161053934 | A>C | SNV | MAP3K4 : Intron Variant | AD |
rs9295134 | chr6:161029496 | C>T | SNV | MAP3K4 : Intron Variant | AD |
rs12188645 | chr5:160869226 | C>T | SNV | ATP10B : Intron Variant | ND |
rs17220405 | chr2:160752258 | C>T | SNV | Intergenic | AD |
rs3795324 | chr1:160673321 | A>C | SNV | Intergenic | AD |
rs4533480 | chr2:160581469 | A>G | SNV | LOC105373718 : Intron Variant | CD |
rs7603576 | chr2:160575093 | A>G | SNV | LOC105373718 : Intron Variant | AD |
rs11681327 | chr2:160568173 | A>G | SNV | LOC105373718 : Intron Variant | AD |
rs9967749 | chr2:160563668 | A>G | SNV | LOC105373718 : Intron Variant | AD |
rs13410476 | chr2:160554031 | G>A | SNV | Intergenic | AD |
rs13034284 | chr2:160553048 | C>T | SNV | Intergenic | AD |
rs7598938 | chr2:160550282 | C>T | SNV | Intergenic | AD |
rs6432628 | chr2:160538677 | C>T | SNV | Intergenic | AD |
rs13382644 | chr2:160530218 | G>A | SNV | Intergenic | AD |
rs1457805 | chr4:159828111 | C>A | SNV | LOC107986324 : Intron Variant | AD |
rs17729321 | chr5:159560721 | T>C | SNV | LOC105377684 : Intron Variant | ND |
rs1433048 | chr5:159328837 | G>A | SNV | IL12B : Intron Variant | AD |
rs2595248 | chr3:159300738 | T>C | SNV | SCHIP1 : Intron Variant IQCJ-SCHIP1 : Intron Variant | ND |
rs7721001 | chr5:159223806 | C>T | SNV | Intergenic | AD |
rs6897374 | chr5:159114192 | C>A | SNV | LOC101927740 : Intron Variant | AD |
rs890622 | chr2:159108877 | G>C | SNV | TANC1 : Intron Variant | ND |
rs13174549 | chr5:159035468 | C>T | SNV | EBF1 : Intron Variant | AD |
rs939998 | chr2:158914458 | C>T | SNV | Intergenic | AD |
rs13035632 | chr2:158893786 | T>C | SNV | Intergenic | AD |
rs10489982 | chr2:158707938 | T>C | SNV | LOC100129029 : Intron Variant | AD |
rs403334 | chr5:158669643 | T>G | SNV | Intergenic | AD |
rs113942939 | chr5:158659196 | G>A | SNV | Intergenic | AD |
rs12724903 | chr1:158609075 | A>C | SNV | Intergenic | AD |
rs17421757 | chr2:158602089 | G>A / G>C | SNV | PKP4 : Intron Variant | AD |
rs7801395 | chr7:158497735 | T>C | SNV | PTPRN2 : Intron Variant | ND |
rs2602189 | chr2:158284712 | A>C | SNV | CCDC148 : Intron Variant | AD |
rs7607379 | chr2:158071694 | C>T | SNV | UPP2 : Intron Variant | AD |
rs1750034 | chr6:158059112 | A>C | SNV | SYNJ2 : Intron Variant | AD |
rs11772608 | chr7:158026633 | T>C | SNV | PTPRN2 : Intron Variant | AD |
rs9365674 | chr6:157990124 | C>T | SNV | SYNJ2 : Intron Variant | AD |
rs2164220 | chr7:157962533 | C>T | SNV | PTPRN2 : Intron Variant | ND |
rs2241749 | chr7:157950773 | G>A | SNV | PTPRN2 : Intron Variant | ND |
rs12123554 | chr1:157935353 | T>C | SNV | LOC105371458 : Intron Variant | AD |
rs1638755 | chr7:157760120 | C>T | SNV | PTPRN2 : Intron Variant | ND |
rs11764539 | chr7:157666180 | T>C | SNV | PTPRN2 : Intron Variant | ND |
rs2778010 | chr1:157651723 | T>C | SNV | Intergenic | AD |
rs741000 | chr7:157485134 | C>T | SNV | LOC101927914 : Intron Variant | AD |
rs13190673 | chr5:157244863 | C>A | SNV | ITK : Intron Variant | AD |
rs1571045 | chr1:157096337 | C>T | SNV | ETV3L : Intron Variant | AD |
rs7715848 | chr5:156974467 | C>G | SNV | Intergenic | AD |
rs6883317 | chr5:156971242 | G>A | SNV | Intergenic | AD |
rs10043150 | chr5:156969464 | C>A | SNV | Intergenic | AD |
rs62382402 | chr5:156964807 | C>T | SNV | TIMD4 : 2KB Upstream Variant | AD |
rs17053982 | chr5:156861811 | G>A | SNV | Intergenic | AD |
rs11683474 | chr2:156816316 | A>T | SNV | LOC107985955 : Intron Variant | ND |
rs12651147 | chr4:156791807 | C>T | SNV | PDGFC : Intron Variant | AD |
rs157672 | chr5:156713071 | C>T | SNV | SGCD : Intron Variant LOC105377673 : Intron Variant | AD |
rs10515737 | chr5:156595519 | A>C | SNV | SGCD : Intron Variant | AD |
rs10515739 | chr5:156590621 | T>C | SNV | SGCD : Intron Variant | AD |
rs17053572 | chr5:156467487 | A>G | SNV | SGCD : Intron Variant | ND |
rs115182184 | chr2:156342049 | G>A | SNV | Intergenic | AD |
rs6767209 | chr3:156290184 | G>A | SNV | KCNAB1 : Intron Variant | AD |
rs4446619 | chr7:156249549 | G>A | SNV | Intergenic | AD |
rs1052067 | chr1:156236330 | G>A | SNV | PMF1 : Missense Variant PMF1-BGLAP : Missense Variant | AD |
rs2241109 | chr1:156203291 | C>T | SNV | SLC25A44 : Intron Variant | AD |
rs1353812 | chr3:156189951 | A>C / A>T | SNV | KCNAB1 : Intron Variant | ND |
rs9397906 | chr6:156171540 | G>A | SNV | LOC101928923 : Intron Variant | AD |
rs5027023 | chr4:156168453 | C>A | SNV | Intergenic | AD |
rs1449675 | chr6:156021488 | T>C | SNV | LOC101928923 : Intron Variant | AD |
rs1449679 | chr6:156014355 | G>A | SNV | LOC101928923 : Intron Variant | AD |
rs11589188 | chr1:156002096 | T>C | SNV | LOC107985208 : Intron Variant LOC107985210 : 500B Downstream Variant | AD |
rs9371951 | chr6:155993786 | T>C | SNV | LOC101928923 : Intron Variant | AD |
rs9397270 | chr6:155842664 | T>C | SNV | LOC101928923 : Intron Variant LOC105378072 : Intron Variant | AD |
rs11134474 | chr5:155775518 | A>G | SNV | SGCD : Intron Variant | ND |
rs4585515 | chr5:155687216 | G>A | SNV | Intergenic | AD |
rs2677485 | chr2:155678644 | T>C | SNV | Intergenic | AD |
rs4407211 | chr2:155650004 | T>C | SNV | LOC107985953 : Intron Variant | AD |
rs6459707 | chr7:155512409 | C>T | SNV | CNPY1 : Intron Variant | ND |
rs6971850 | chr7:155511477 | A>C | SNV | CNPY1 : Intron Variant | ND |
rs4691643 | chr4:155457416 | C>T | SNV | Intergenic | AD |
rs10497148 | chr2:155226832 | A>G | SNV | Intergenic | AD |
rs2969540 | chr7:155109147 | C>T | SNV | Intergenic | AD |
rs3807235 | chr7:154685668 | A>C | SNV | DPP6 : Intron Variant | AD |
rs2072661 | chr1:154576404 | G>A | SNV | CHRNB2 : Non Coding Transcript Variant | ND |
rs12392447 | chrX:154496001 | A>G | SNV | Intergenic | AD |
rs9640200 | chr7:154470566 | T>G | SNV | DPP6 : Intron Variant | ND |
rs4240872 | chr1:154463719 | C>T | SNV | IL6R : Intron Variant | AD |
rs10037670 | chr5:154431930 | A>G | SNV | SAP30L-AS1 : Intron Variant | AD |
rs17654071 | chr1:154396776 | A>G | SNV | Intergenic | AD |
rs11582424 | chr1:154391509 | A>C | SNV | Intergenic | AD |
rs12526737 | chr6:154387499 | T>C | SNV | Intergenic | AD |
rs6464419 | chr7:154386240 | A>G | SNV | DPP6 : Intron Variant | ND |
rs1760803 | chr1:154285418 | A>T | SNV | Intergenic | ND |
rs10274025 | chr7:154270195 | G>A | SNV | DPP6 : Intron Variant | ND |
rs890793 | chr5:154194378 | C>G / C>T | SNV | GALNT10 : Intron Variant | AD |
rs790919 | chr6:153977740 | A>T | SNV | Intergenic | ND |
rs712241 | chr6:153972045 | G>C / G>T | SNV | Intergenic | ND |
rs2963998 | chr5:153797493 | C>A / C>T | SNV | GRIA1 : Intron Variant | AD |
rs7445323 | chr5:153757225 | T>G | SNV | GRIA1 : Intron Variant | AD |
rs4128572 | chr5:153749155 | A>G | SNV | GRIA1 : Intron Variant | AD |
rs6889794 | chr5:153743895 | A>G | SNV | GRIA1 : Intron Variant | AD |
rs4273649 | chr5:153740488 | A>C / A>G / A>T | SNV | GRIA1 : Intron Variant | AD |
rs4145338 | chr4:153733171 | T>C | SNV | RNF175 : Intron Variant LOC105377499 : Intron Variant | AD |
rs2033831 | chr4:153637999 | A>G | SNV | KIAA0922 : 500B Downstream Variant | AD |
rs3961460 | chr3:153598435 | T>C | SNV | LOC105374165 : Intron Variant | AD |
rs1973372 | chr5:153582064 | C>T | SNV | GRIA1 : Intron Variant | AD |
rs13418009 | chr2:153416028 | A>G | SNV | Intergenic | AD |
rs12027903 | chr1:153355280 | G>T | SNV | Intergenic | AD |
rs9822442 | chr3:153309700 | T>C | SNV | Intergenic | AD |
rs6799941 | chr3:153281590 | T>G | SNV | Intergenic | AD |
rs4285401 | chr7:153181248 | A>G | SNV | LOC102723686 : 2KB Upstream Variant | ND |
rs7795531 | chr7:153171421 | C>T | SNV | Intergenic | AD |
rs10259781 | chr7:153169940 | G>A | SNV | Intergenic | AD |
rs6832907 | chr4:153061733 | A>G | SNV | Intergenic | AD |
rs12060809 | chr1:152676474 | T>C | SNV | LCE2C : 3 Prime UTR Variant | AD |
rs12096806 | chr1:152670684 | G>A | SNV | Intergenic | AD |
rs10888505 | chr1:152652672 | A>G | SNV | Intergenic | AD |
rs1844895 | chrX:152132250 | C>T | SNV | MAGEA10-MAGEA5 : Intron Variant | AD |
rs154101 | chr5:152103802 | A>C / A>G / A>T | SNV | CTB-12O2.1 : Intron Variant | ND |
rs29854 | chr5:152087407 | T>C | SNV | CTB-12O2.1 : Intron Variant | ND |
rs10952334 | chr7:151956550 | G>C | SNV | GALNTL5 : Non Coding Transcript Variant LOC105375570 : 2KB Upstream Variant LOC105375571 : 2KB Upstream Variant | AD |
rs6902771 | chr6:151836746 | C>T | SNV | ESR1 : Intron Variant | AD |
rs9874357 | chr3:151796917 | T>C | SNV | AADACL2-AS1 : Intron Variant LOC105374160 : Intron Variant | AD |
rs12472627 | chr2:151776600 | C>T | SNV | LOC101929356 : Non Coding Transcript Variant | AD |
rs4725432 | chr7:151776332 | C>A | SNV | PRKAG2 : Intron Variant | ND |
rs10224002 | chr7:151717955 | A>G | SNV | PRKAG2 : Intron Variant | AD |
rs2302530 | chr7:151570311 | G>A | SNV | PRKAG2 : Intron Variant | ND |
rs13031275 | chr2:151489980 | A>C | SNV | NEB : Synonymous Variant RIF1 : Intron Variant | AD |
rs168700 | chr5:151239441 | G>A | SNV | Intergenic | AD |
rs6933598 | chr6:150938634 | C>G | SNV | MTHFD1L : Intron Variant | AD |
rs11099777 | chr4:150854107 | G>A | SNV | LRBA : Intron Variant | AD |
rs17427389 | chr6:150841979 | G>A | SNV | PLEKHG1 : 3 Prime UTR Variant | AD | ND |
rs9640279 | chr7:150571010 | G>T | SNV | GIMAP4 : Intron Variant | AD |
rs939958 | chr7:150560680 | C>A / C>T | SNV | LOC107986860 : Intron Variant | AD |
rs13208542 | chr6:150535634 | G>C | SNV | Intergenic | ND |
rs13197942 | chr6:150404961 | G>T | SNV | IYD : 500B Downstream Variant | AD |
rs10263613 | chr7:150363074 | G>A | SNV | LOC105375563 : Non Coding Transcript Variant | AD |
rs6716455 | chr2:150269889 | G>A | SNV | LOC105373684 : Intron Variant | AD |
rs330630 | chr2:150092189 | T>C | SNV | Intergenic | AD |
rs6608304 | chrX:150065001 | G>A | SNV | Intergenic | AD |
rs17079029 | chr6:149918194 | C>T | SNV | RAET1G : Synonymous Variant RAET1E-AS1 : Intron Variant | AD |
rs880770 | chr5:149775272 | G>A | SNV | PPARGC1B : Intron Variant | AD |
rs4705371 | chr5:149758061 | C>A | SNV | PPARGC1B : Intron Variant | AD |
rs4705088 | chr5:149757069 | T>G | SNV | PPARGC1B : Intron Variant | AD |
rs7638140 | chr3:149629784 | G>A | SNV | WWTR1 : Intron Variant | AD |
rs6790596 | chr3:149629260 | G>A | SNV | WWTR1 : Intron Variant | AD |
rs9857773 | chr3:149626828 | C>A | SNV | WWTR1 : Intron Variant | AD |
rs1344815 | chr3:149623026 | A>G | SNV | WWTR1 : Intron Variant | AD |
rs3747443 | chrX:149541185 | A>G | SNV | CXorf40A : Intron Variant LINC00893 : 2KB Upstream Variant | AD |
rs1120211 | chrX:149385781 | A>C / A>G | SNV | Intergenic | ND |
rs17487852 | chr4:149207696 | A>G | SNV | LOC101927849 : Intron Variant | AD |
rs7797617 | chr7:149088629 | A>C | SNV | ZNF786 : Intron Variant | AD |
rs12113550 | chr7:149081590 | A>G | SNV | ZNF786 : Intron Variant | AD |
rs6973937 | chr7:149074254 | C>T | SNV | ZNF786 : Intron Variant | AD |
rs10201643 | chr2:149049127 | T>G | SNV | LYPD6B : Intron Variant | AD |
rs16822509 | chr2:149038210 | T>C | SNV | LYPD6B : 2KB Upstream Variant | AD |
rs10929935 | chr2:149036100 | T>C | SNV | Intergenic | AD |
rs7577450 | chr2:149019447 | A>G | SNV | KIF5C : Intron Variant | AD |
rs2486416 | chr6:149014873 | C>T | SNV | UST : Intron Variant | AD |
rs2486396 | chr6:149000610 | C>T | SNV | UST : Intron Variant | AD |
rs11965507 | chr6:148874287 | G>A | SNV | UST : Intron Variant | AD |
rs1042718 | chr5:148827354 | C>A / C>T | SNV | ADRB2 : Missense Variant | AD |
rs1042717 | chr5:148827083 | G>A / G>C | SNV | ADRB2 : Synonymous Variant | AD |
rs7753810 | chr6:148791620 | T>G | SNV | UST : Intron Variant | ND |
rs6420783 | chr6:148631952 | C>A | SNV | Intergenic | AD |
rs73017046 | chr6:148560592 | G>A | SNV | Intergenic | AD |
rs5522 | chr4:148436323 | C>T | SNV | NR3C2 : Missense Variant | ND |
rs5525 | chr4:148435364 | A>C / A>G | SNV | NR3C2 : Missense Variant | ND |
rs16860281 | chr3:148277560 | T>C | SNV | Intergenic | ND |
rs10037701 | chr5:148161600 | C>T | SNV | SPINK14 : Intron Variant | AD |
rs1117507 | chr5:148157593 | A>G | SNV | SPINK14 : Intron Variant | AD |
rs2061668 | chr3:147995192 | C>A | SNV | Intergenic | AD |
rs11771941 | chr7:147982443 | G>A | SNV | CNTNAP2 : Intron Variant | ND |
rs2178771 | chr7:147966400 | T>G | SNV | CNTNAP2 : Intron Variant | ND |
rs2707592 | chr7:147963361 | A>G | SNV | CNTNAP2 : Intron Variant | ND |
rs10515595 | chr5:147862163 | C>T | SNV | C5orf46 : Intron Variant | AD |
rs851712 | chr7:147831639 | A>G | SNV | CNTNAP2 : Intron Variant | ND |
rs964170 | chr4:147774805 | G>T | SNV | ARHGAP10 : Intron Variant | ND |
rs9322108 | chr6:147724045 | A>G | SNV | SAMD5 : Intron Variant | AD |
rs13374159 | chr1:147670335 | C>T | SNV | ACP6 : Non Coding Transcript Variant | AD |
rs844604 | chr6:147603319 | T>G | SNV | SAMD5 : Intron Variant | ND |
rs702354 | chr6:147601419 | T>C | SNV | SAMD5 : Intron Variant | ND |
rs844613 | chr6:147597446 | G>C | SNV | SAMD5 : Intron Variant | ND |
rs1944645 | chr6:147594330 | A>C | SNV | SAMD5 : Intron Variant | ND |
rs844577 | chr6:147592924 | A>T | SNV | SAMD5 : Intron Variant | ND |
rs844574 | chr6:147591579 | A>C | SNV | SAMD5 : Intron Variant | ND |
rs844568 | chr6:147591295 | G>A / G>T | SNV | SAMD5 : Intron Variant | ND |
rs844563 | chr6:147588032 | T>C | SNV | SAMD5 : Intron Variant | ND |
rs844562 | chr6:147587859 | T>C | SNV | SAMD5 : Intron Variant | ND |
rs702353 | chr6:147585618 | G>A | SNV | SAMD5 : Intron Variant | ND |
rs844557 | chr6:147585145 | T>C | SNV | SAMD5 : Intron Variant | ND |
rs844625 | chr6:147578081 | T>C | SNV | SAMD5 : Intron Variant | ND |
rs716703 | chr1:147549375 | C>T | SNV | BCL9 : Intron Variant | ND |
rs12072533 | chr1:147545754 | A>C | SNV | BCL9 : Intron Variant | ND |
rs389674 | chr6:147491880 | C>T | SNV | Intergenic | ND |
rs325127 | chr6:147485583 | A>T | SNV | Intergenic | ND |
rs11167990 | chr5:147412193 | A>G | SNV | DPYSL3 : Intron Variant | AD |
rs13170855 | chr5:147295570 | C>T | SNV | STK32A : Intron Variant | ND |
rs10279700 | chr7:147271203 | T>C | SNV | CNTNAP2 : Intron Variant | AD |
rs5904713 | chrX:147159661 | G>T | SNV | Intergenic | ND |
rs1911588 | chr4:147099992 | T>C | SNV | Intergenic | AD |
rs1864982 | chr5:146941260 | G>T | SNV | PPP2R2B : Intron Variant | AD |
rs10037107 | chr5:146849539 | A>G | SNV | PPP2R2B : Intron Variant | AD |
rs4525630 | chr2:146752321 | C>G / C>T | SNV | Intergenic | ND |
rs970674 | chr4:146629922 | G>A | SNV | Intergenic | AD |
rs1870424 | chr3:146514201 | T>C | SNV | Intergenic | AD |
rs11692798 | chr2:146240072 | C>T | SNV | LOC105373667 : Intron Variant | AD |
rs6661602 | chr1:146006739 | A>G | SNV | Intergenic | AD |
rs6424380 | chr1:145863686 | G>A | SNV | Intergenic | AD |
rs1027841 | chr4:145847922 | G>A | SNV | ZNF827 : Intron Variant | AD |
rs2381750 | chr2:145624668 | G>A / G>T | SNV | LOC105373664 : Intron Variant | AD |
rs13109195 | chr4:145448604 | T>C | SNV | Intergenic | AD |
rs10496968 | chr2:144766679 | C>T | SNV | TEX41 : Intron Variant | AD |
rs11883829 | chr2:144762056 | A>G | SNV | TEX41 : Intron Variant | AD |
rs1351734 | chr2:144729026 | T>C | SNV | TEX41 : Intron Variant | AD |
rs7762384 | chr6:144719159 | C>A | SNV | UTRN : Intron Variant | AD |
rs4471836 | chr2:144717578 | G>A | SNV | TEX41 : Intron Variant | AD |
rs10496966 | chr2:144701195 | A>G | SNV | TEX41 : Intron Variant | AD |
rs2195115 | chr2:144688638 | G>A | SNV | TEX41 : Intron Variant | AD |
rs980772 | chr2:144684623 | G>A / G>T | SNV | TEX41 : Intron Variant | AD |
rs10224675 | chr7:144595669 | A>G | SNV | TPK1 : Intron Variant | AD |
rs12664298 | chr6:144362485 | G>A | SNV | UTRN : Intron Variant | AD |
rs787176 | chr2:143910681 | C>T | SNV | Intergenic | ND |
rs787151 | chr2:143898268 | A>G | SNV | Intergenic | ND |
rs13018437 | chr2:143856197 | G>A | SNV | Intergenic | ND |
rs4839669 | chr3:143823101 | G>C | SNV | SLC9A9 : Intron Variant | ND |
rs6931825 | chr6:143758651 | A>C | SNV | PHACTR2 : Intron Variant | AD |
rs9390132 | chr6:143740552 | G>A | SNV | PHACTR2 : Intron Variant | AD |
rs960710 | chr6:143739821 | G>A | SNV | PHACTR2 : Intron Variant | AD |
rs1992864 | chr3:143687600 | C>T | SNV | SLC9A9 : Intron Variant | ND |
rs12679735 | chr8:143651635 | C>T | SNV | ZNF623 : 3 Prime UTR Variant | AD |
rs3750204 | chr8:143650280 | G>A / G>C / G>T | SNV | ZNF623 : Synonymous Variant | AD |
rs11693600 | chr2:143622973 | C>T | SNV | ARHGAP15 : Intron Variant | ND |
rs10496950 | chr2:143615404 | C>G | SNV | ARHGAP15 : Intron Variant | ND |
rs9289666 | chr3:143526140 | A>G | SNV | SLC9A9 : Intron Variant | ND |
rs838621 | chr3:143469211 | C>T | SNV | SLC9A9 : Intron Variant | AD |
rs838610 | chr3:143459684 | A>C | SNV | SLC9A9 : Intron Variant | AD |
rs1723034 | chr3:143458406 | C>T | SNV | SLC9A9 : Intron Variant | AD |
rs2496590 | chr6:143414625 | T>A / T>C | SNV | Intergenic | AD |
rs868702 | chr3:143366503 | G>A | SNV | SLC9A9 : Intron Variant | AD |
rs6775025 | chr3:143350462 | T>C | SNV | SLC9A9 : Intron Variant | ND |
rs10446322 | chr3:143349408 | A>G | SNV | SLC9A9 : Intron Variant | AD |
rs7431637 | chr3:143330927 | T>C | SNV | SLC9A9 : Intron Variant | AD |
rs7639109 | chr3:143275352 | C>T | SNV | SLC9A9 : Intron Variant | AD |
rs12703516 | chr7:143142075 | A>G | SNV | Intergenic | AD |
rs16858596 | chr2:143132712 | G>A | SNV | ARHGAP15 : Intron Variant | AD |
rs7846671 | chr8:143102549 | A>G | SNV | Intergenic | AD |
rs2095369 | chr6:142949079 | A>G | SNV | LOC107986655 : Non Coding Transcript Variant | AD |
rs7768492 | chr6:142824095 | T>G | SNV | HIVEP2 : Intron Variant | AD |
rs9841007 | chr3:142822845 | T>C | SNV | PCOLCE2 : Intron Variant | AD |
rs9815607 | chr3:142791506 | G>A | SNV | TRPC1 : Intron Variant | AD |
rs6951271 | chr7:142726593 | A>C / A>T | SNV | Intergenic | AD |
rs13094259 | chr3:142725783 | G>T | SNV | TRPC1 : Intron Variant | AD |
rs1916998 | chr5:142694567 | G>T | SNV | FGF1 : Intron Variant | ND |
rs7835613 | chr8:142601067 | G>A | SNV | Intergenic | ND |
rs7636909 | chr3:142541720 | A>G | SNV | ATR : Intron Variant | ND |
rs6583607 | chr8:142243038 | T>C | SNV | TSNARE1 : Intron Variant | AD |
rs9308148 | chr4:142177786 | A>G | SNV | INPP4B : Intron Variant | AD |
rs1062158 | chr5:142143435 | C>A / C>T | SNV | NDFIP1 : Intron Variant | AD |
rs7733850 | chr5:142135999 | C>T | SNV | NDFIP1 : Intron Variant | AD |
rs7709361 | chr5:142134289 | T>C | SNV | NDFIP1 : Intron Variant | AD |
rs6863411 | chr5:142133639 | A>T | SNV | NDFIP1 : Intron Variant | AD |
rs11749731 | chr5:142120871 | A>C / A>G | SNV | NDFIP1 : Intron Variant | AD |
rs4912622 | chr5:142111022 | G>A | SNV | NDFIP1 : Intron Variant | AD |
rs9324865 | chr5:142109227 | T>C | SNV | NDFIP1 : Intron Variant | AD |
rs11167764 | chr5:142099500 | A>C | SNV | LOC105378204 : Intron Variant | AD |
rs4276595 | chr7:142065905 | T>C | SNV | MGAM : Intron Variant | ND |
rs2204607 | chr7:142009894 | C>T | SNV | MGAM : Intron Variant | AD |
rs6947481 | chr7:141993008 | T>G | SNV | MGAM : Intron Variant | ND |
rs17097654 | chr5:141808749 | G>T | SNV | LOC107986454 : Non Coding Transcript Variant | ND |
rs10928122 | chr2:141772551 | G>A / G>T | SNV | LRP1B : Intron Variant | AD |
rs1519548 | chr4:141609456 | C>T | SNV | Intergenic | AD |
rs7558514 | chr2:141219604 | G>A | SNV | LRP1B : Intron Variant | AD |
rs307766 | chr8:141141614 | C>T | SNV | DENND3 : Intron Variant | AD |
rs6429856 | chr2:141022386 | G>A | SNV | LRP1B : Intron Variant | AD |
rs347964 | chr3:140588564 | A>G | SNV | Intergenic | AD |
rs3923350 | chr2:140482029 | G>T | SNV | LRP1B : Intron Variant | ND |
rs9640467 | chr7:140396403 | C>T | SNV | SLC37A3 : Intron Variant | AD |
rs9640465 | chr7:140396357 | C>T | SNV | SLC37A3 : Intron Variant | AD |
rs6947516 | chr7:140380048 | G>A | SNV | SLC37A3 : Intron Variant | AD |
rs6955063 | chr7:140377628 | A>C | SNV | SLC37A3 : Intron Variant | AD |
rs7777468 | chr7:140371515 | C>T | SNV | SLC37A3 : Intron Variant | AD |
rs6439914 | chr3:140290378 | A>G | SNV | CLSTN2 : Intron Variant | AD |
rs4077501 | chr3:140278306 | T>C | SNV | CLSTN2 : Intron Variant | AD |
rs7626587 | chr3:140274852 | A>G | SNV | CLSTN2 : Intron Variant | AD |
rs7014855 | chr8:140247165 | C>T | SNV | TRAPPC9 : Intron Variant | AD |
rs6798469 | chr3:140182692 | C>T | SNV | CLSTN2 : Intron Variant | ND |
rs16849613 | chr3:139979746 | T>A | SNV | CLSTN2 : Intron Variant | ND |
rs4725563 | chr7:139954457 | C>T | SNV | TBXAS1 : Intron Variant | ND |
rs3015437 | chr6:139803938 | A>G | SNV | LOC100132735 : Intron Variant | ND |
rs6958644 | chr7:139796416 | A>G | SNV | TBXAS1 : Intron Variant | AD |
rs11773968 | chr8:139758768 | G>T | SNV | TRAPPC9 : Intron Variant | AD |
rs10935348 | chr3:139728658 | C>A | SNV | Intergenic | AD |
rs10935342 | chr3:139686500 | T>C | SNV | Intergenic | AD |
rs10954654 | chr7:139674341 | C>T | SNV | HIPK2 : Intron Variant | AD |
rs2014712 | chr8:139628391 | C>G / C>T | SNV | KCNK9 : Intron Variant | AD |
rs2542435 | chr8:139591259 | G>A | SNV | Intergenic | AD |
rs11688290 | chr2:139051336 | C>T | SNV | Intergenic | AD |
rs1605136 | chr2:139046571 | A>G / A>T | SNV | Intergenic | AD |
rs1505846 | chr2:139020712 | C>T | SNV | Intergenic | AD |
rs3922799 | chr2:139001336 | G>A / G>T | SNV | Intergenic | AD |
rs112525781 | chr2:138961777 | C>T | SNV | LOC105373640 : Intron Variant | AD |
rs10803574 | chr2:138953293 | G>A | SNV | LOC105373640 : Intron Variant | AD |
rs2272432 | chr6:138917462 | G>T | SNV | REPS1 : Intron Variant | AD |
rs9636231 | chr2:138914385 | G>A | SNV | LOC105373639 : Intron Variant | AD |
rs10499204 | chr6:138895289 | T>C | SNV | ECT2L : Intron Variant LOC107986650 : Intron Variant | AD |
rs12493155 | chr3:138681490 | C>T | SNV | PIK3CB : Intron Variant | AD |
rs529615 | chr3:138594992 | C>T | SNV | CEP70 : 2KB Upstream Variant | AD |
rs7799136 | chr7:138591889 | C>T | SNV | SVOPL : 3 Prime UTR Variant | ND |
rs1199335 | chr3:138370982 | A>G | SNV | MRAS : Intron Variant | AD |
rs11723658 | chr4:138236842 | C>A | SNV | SLC7A11 : Intron Variant | AD |
rs2484066 | chr6:138095981 | T>G | SNV | PERP : Intron Variant | AD |
rs2506843 | chr6:138095943 | C>G | SNV | PERP : Intron Variant | AD |
rs11971315 | chr7:138018590 | G>A | SNV | Intergenic | AD |
rs6439772 | chr3:137962606 | A>G | SNV | Intergenic | AD |
rs2375511 | chr2:137491882 | C>A | SNV | THSD7B : Intron Variant | AD |
rs1869324 | chr2:137469872 | G>A | SNV | THSD7B : Intron Variant | AD |
rs7804771 | chr7:137447847 | C>G | SNV | DGKI : Intron Variant | ND |
rs5931118 | chrX:137291555 | G>A | SNV | Intergenic | AD |
rs11099428 | chr4:137201200 | C>T | SNV | LOC105377441 : Intron Variant | AD |
rs1554075 | chr4:137198353 | T>C | SNV | LOC729307 : Non Coding Transcript Variant LOC105377441 : Intron Variant | AD |
rs6833974 | chr4:137197929 | A>G | SNV | LOC729307 : Non Coding Transcript Variant LOC105377441 : Intron Variant | AD |
rs11937897 | chr4:137197806 | A>G | SNV | LOC729307 : Non Coding Transcript Variant LOC105377441 : Intron Variant | AD |
rs13148112 | chr4:137197751 | G>A | SNV | LOC729307 : Non Coding Transcript Variant LOC105377441 : Intron Variant | AD |
rs2406485 | chr4:137191836 | T>C | SNV | LOC105377441 : Intron Variant LOC729307 : 2KB Upstream Variant | AD |
rs17065341 | chr9:137084167 | A>G | SNV | UAP1L1 : 3 Prime UTR Variant | AD |
rs1744061 | chr6:137003518 | C>T | SNV | IL20RA : Intron Variant | AD |
rs11145948 | chr9:136963460 | G>A | SNV | Intergenic | AD |
rs17168826 | chr7:136951740 | C>T | SNV | CHRM2 : Intron Variant LOC349160 : Intron Variant | AD |
rs6560652 | chr9:136936488 | T>C | SNV | Intergenic | AD |
rs2386140 | chr9:136929170 | A>G | SNV | Intergenic | AD |
rs10007934 | chr4:136903447 | G>A | SNV | LOC105377441 : Intron Variant | AD |
rs7041558 | chr9:136664675 | A>G | SNV | EGFL7 : Intron Variant | AD |
rs5930973 | chrX:136649989 | G>A | SNV | CD40LG : Intron Variant | AD |
rs2033172 | chr2:136482734 | A>G | SNV | Intergenic | AD |
rs10496746 | chr2:136449512 | C>T | SNV | Intergenic | AD |
rs16834223 | chr2:136436866 | A>G | SNV | Intergenic | AD |
rs2673931 | chr5:136353748 | C>T | SNV | TRPC7 : Intron Variant | ND |
rs2546657 | chr5:136348047 | T>A | SNV | TRPC7 : Intron Variant | ND |
rs4976489 | chr5:136343269 | C>T | SNV | TRPC7 : Intron Variant | ND |
rs1499764 | chr5:136328500 | T>C | SNV | TRPC7 : Intron Variant | ND |
rs2216640 | chr5:136319413 | C>T | SNV | TRPC7 : Intron Variant | ND |
rs10070699 | chr5:136316252 | G>A | SNV | TRPC7 : Intron Variant TRPC7-AS2 : 500B Downstream Variant | ND |
rs16905615 | chr8:136315901 | G>A | SNV | Intergenic | AD |
rs4976485 | chr5:136314610 | A>G | SNV | TRPC7 : Intron Variant TRPC7-AS2 : Intron Variant | ND |
rs11675636 | chr2:136280972 | A>T | SNV | Intergenic | AD |
rs4477975 | chr2:136251436 | A>G | SNV | Intergenic | AD |
rs7765567 | chr6:136075736 | A>G | SNV | PDE7B : Intron Variant LOC644135 : Intron Variant | AD |
rs2011946 | chr2:136060046 | C>A | SNV | Intergenic | AD |
rs6921041 | chr6:136049520 | T>G | SNV | PDE7B : Intron Variant LOC644135 : Intron Variant | AD |
rs2107331 | chr5:136041660 | C>A | SNV | TGFBI : Intron Variant | AD |
rs1401543 | chr3:135868969 | T>C | SNV | Intergenic | AD |
rs17168705 | chr5:135594315 | C>A | SNV | SLC25A48 : Intron Variant | AD |
rs17168703 | chr5:135594000 | A>G | SNV | SLC25A48 : Intron Variant | AD |
rs7045084 | chr9:135545890 | C>T | SNV | OBP2A : 5 Prime UTR Variant | ND |
rs6997956 | chr8:135472147 | T>A | SNV | KHDRBS3 : Intron Variant | ND |
rs7712997 | chr5:135327407 | G>T | SNV | C5orf66 : Intron Variant | AD |
rs17235985 | chr7:135309545 | G>T | SNV | LOC107984123 : Intron Variant | AD |
rs4841962 | chr9:135303357 | A>C / A>T | SNV | Intergenic | AD |
rs8179953 | chr3:135235483 | G>A | SNV | EPHB1 : Intron Variant | ND |
rs2404646 | chr4:135165126 | C>G | SNV | Intergenic | ND |
rs4909801 | chr8:134866916 | T>C | SNV | LOC101927845 : Intron Variant | AD |
rs11224040 | chr11:134857954 | T>C | SNV | Intergenic | AD |
rs7717860 | chr5:134854535 | C>A | SNV | C5orf24 : Intron Variant | AD |
rs4504708 | chr9:134844698 | G>T | SNV | COL5A1 : 3 Prime UTR Variant LOC101448202 : Intron Variant | AD |
rs6904528 | chr6:134827811 | A>T | SNV | LOC101928277 : Intron Variant | AD |
rs200733877 | chr4:134814437 | delT | Deletion | Intergenic | AD |
rs13144694 | chr4:134814436 | A>G | SNV | Intergenic | AD |
rs11918092 | chr3:134794514 | C>A | SNV | EPHB1 : Intron Variant | AD |
rs2347896 | chr7:134780643 | C>A | SNV | CALD1 : Intron Variant | AD |
rs548172 | chr4:134765322 | T>C | SNV | Intergenic | AD |
rs7749709 | chr6:134758479 | G>A | SNV | LOC101928277 : Intron Variant | ND |
rs10935129 | chr3:134750689 | T>A | SNV | Intergenic | AD |
rs10079478 | chr5:134505105 | T>C | SNV | LOC101927934 : 2KB Upstream Variant | AD |
rs9409931 | chr9:134450911 | T>C | SNV | Intergenic | AD |
rs9409930 | chr9:134450622 | T>C | SNV | Intergenic | AD |
rs11103603 | chr9:134449754 | T>C | SNV | Intergenic | AD |
rs7928758 | chr11:134396073 | T>G | SNV | B3GAT1 : Intron Variant | AD |
rs393459 | chr7:134285692 | T>G | SNV | Intergenic | AD |
rs11825659 | chr11:133925624 | A>G | SNV | IGSF9B : Intron Variant | AD |
rs731590 | chr5:133888397 | C>T | SNV | Intergenic | AD |
rs1880663 | chr3:133862615 | A>G | SNV | RAB6B : Intron Variant | AD |
rs17310798 | chr3:133844095 | T>C | SNV | RAB6B : Intron Variant | AD |
rs2692672 | chr3:133836656 | T>G | SNV | RAB6B : Intron Variant | AD |
rs6793673 | chr3:133834428 | C>T | SNV | RAB6B : Intron Variant | AD |
rs11921187 | chr3:133832798 | T>C | SNV | RAB6B : Intron Variant | AD |
rs2293374 | chr3:133828401 | G>A | SNV | RAB6B : 3 Prime UTR Variant | AD |
rs12637730 | chr3:133827453 | C>T | SNV | RAB6B : 3 Prime UTR Variant | AD |
rs17310413 | chr3:133823117 | T>G | SNV | Intergenic | AD |
rs6773354 | chr3:133822930 | C>T | SNV | Intergenic | AD |
rs6439443 | chr3:133822071 | T>C | SNV | Intergenic | AD |
rs17376019 | chr3:133822039 | C>T | SNV | Intergenic | AD |
rs6439442 | chr3:133821515 | A>C | SNV | SRPRB : 500B Downstream Variant | AD |
rs1534166 | chr3:133818223 | A>G | SNV | SRPRB : Intron Variant | AD |
rs1534165 | chr3:133818073 | T>C | SNV | SRPRB : Intron Variant | AD |
rs1464937 | chr3:133817811 | G>C / G>T | SNV | SRPRB : Intron Variant | AD |
rs6439441 | chr3:133810750 | A>G | SNV | SRPRB : Intron Variant | AD |
rs7650925 | chr3:133808325 | G>T | SNV | SRPRB : Intron Variant | AD |
rs3817524 | chr3:133807559 | C>T | SNV | SRPRB : Intron Variant LOC105374116 : 2KB Upstream Variant | AD |
rs1107413 | chr3:133805873 | G>C | SNV | SRPRB : Missense Variant LOC105374116 : 2KB Upstream Variant | AD |
rs12490148 | chr3:133805129 | C>T | SNV | SRPRB : Intron Variant LOC105374116 : Non Coding Transcript Variant | AD |
rs9853615 | chr3:133801137 | A>G | SNV | SRPRB : Intron Variant LOC105374116 : Intron Variant | AD |
rs6794945 | chr3:133799619 | C>T | SNV | SRPRB : Intron Variant LOC105374116 : Intron Variant | AD |
rs9881405 | chr3:133799354 | G>T | SNV | SRPRB : Intron Variant LOC105374116 : Intron Variant | AD |
rs1476118 | chr7:133790019 | C>A / C>T | SNV | EXOC4 : Intron Variant | AD |
rs1830084 | chr3:133789620 | A>T | SNV | SRPRB : Intron Variant LOC105374116 : Intron Variant | AD |
rs9843728 | chr3:133782563 | C>T | SNV | SRPRB : 2KB Upstream Variant | AD |
rs4854762 | chr3:133780219 | G>A | SNV | Intergenic | AD |
rs4854761 | chr3:133779945 | G>A | SNV | Intergenic | AD |
rs4854760 | chr3:133779897 | A>G | SNV | Intergenic | AD |
rs7638018 | chr3:133776617 | A>G | SNV | TF : Intron Variant | AD |
rs1049296 | chr3:133775510 | C>T | SNV | TF : Missense Variant | AD |
rs1525889 | chr3:133771189 | A>C | SNV | TF : Intron Variant | AD |
rs2692695 | chr3:133766610 | A>G | SNV | TF : Intron Variant | AD |
rs41295800 | chr3:133765869-133765874 | delT | Indel | TF : Intron Variant | AD |
rs1525892 | chr3:133765868 | G>A | SNV | TF : Intron Variant | AD |
rs1358024 | chr3:133765344 | C>T | SNV | TF : Intron Variant | AD |
rs3811647 | chr3:133765185 | G>A | SNV | TF : Intron Variant | AD |
rs8177272 | chr3:133764026 | G>A | SNV | TF : Intron Variant | AD |
rs8177252 | chr3:133761330 | C>A / C>G | SNV | TF : Intron Variant | AD |
rs8177240 | chr3:133758857 | T>C / T>G | SNV | TF : Intron Variant | AD |
rs1799899 | chr3:133756968 | G>A | SNV | TF : Missense Variant | AD |
rs1799852 | chr3:133756878 | C>T | SNV | TF : Synonymous Variant | AD |
rs8177220 | chr3:133754781 | G>C / G>T | SNV | TF : Intron Variant | AD |
rs8177213 | chr3:133753383 | A>C | SNV | TF : Intron Variant | AD |
rs8177197 | chr3:133750686 | G>A | SNV | TF : Intron Variant | AD |
rs8177191 | chr3:133749295 | G>A | SNV | TF : Intron Variant | AD |
rs6785596 | chr3:133747613 | T>A | SNV | TF : Intron Variant | AD |
rs6796795 | chr3:133747378 | A>G | SNV | TF : Intron Variant | AD |
rs1800277 | chr3:133747311 | C>T | SNV | TF : Intron Variant | AD |
rs4459901 | chr3:133746855 | T>C | SNV | TF : Intron Variant | AD |
rs8177313 | chr3:133745258 | T>G | SNV | TF : Intron Variant | AD |
rs8177178 | chr3:133744428 | G>A | SNV | TF : Intron Variant | AD |
rs6787177 | chr3:133731876 | C>T | SNV | TF : Intron Variant | AD |
rs7646118 | chr3:133731195 | C>T | SNV | TF : Intron Variant | AD |
rs6439431 | chr3:133729265 | A>C | SNV | TF : Intron Variant | AD |
rs6775042 | chr3:133723401 | G>T | SNV | TF : Intron Variant | AD |
rs6774822 | chr3:133723168 | G>C / G>T | SNV | TF : Intron Variant | AD |
rs7843718 | chr8:133722977 | A>G | SNV | Intergenic | AD |
rs12639304 | chr3:133722750 | A>T | SNV | TF : Intron Variant | AD |
rs11921527 | chr3:133722323 | G>A | SNV | TF : Intron Variant | AD |
rs10935073 | chr3:133720340 | T>C | SNV | TF : Intron Variant | AD |
rs6782523 | chr3:133720073 | C>G / C>T | SNV | TF : Intron Variant | AD |
rs4525863 | chr3:133717292 | C>A | SNV | TF : Intron Variant | AD |
rs9830001 | chr3:133714626 | G>A | SNV | TF : Intron Variant | AD |
rs1901439 | chr2:133679900 | T>C | SNV | Intergenic | AD |
rs10935070 | chr3:133623144 | T>C / T>G | SNV | TOPBP1 : Missense Variant | AD |
rs1444600 | chr3:133569662 | C>T | SNV | Intergenic | AD |
rs4854733 | chr3:133568221 | A>G | SNV | Intergenic | AD |
rs10433415 | chr3:133566686 | G>T | SNV | Intergenic | AD |
rs6778062 | chr3:133548309 | G>C | SNV | Intergenic | AD |
rs872134 | chr3:133546688 | G>T | SNV | Intergenic | AD |
rs7614812 | chr3:133545407 | C>A | SNV | Intergenic | AD |
rs10935068 | chr3:133543963 | T>A | SNV | Intergenic | AD |
rs6763627 | chr3:133543723 | C>G / C>T | SNV | Intergenic | AD |
rs6785365 | chr3:133543601 | A>G | SNV | Intergenic | AD |
rs3860498 | chr3:133541672 | T>A / T>C | SNV | Intergenic | AD |
rs4017074 | chr3:133541583 | T>C | SNV | Intergenic | AD |
rs4854727 | chr3:133539041 | A>G | SNV | Intergenic | AD |
rs4854723 | chr3:133535414 | A>C | SNV | Intergenic | AD |
rs6989475 | chr8:133507022 | A>G | SNV | ST3GAL1 : Intron Variant | AD |
rs2814209 | chr10:133468697 | T>C | SNV | SCART1 : 500B Downstream Variant | AD |
rs11099240 | chr4:133436700 | G>A / G>T | SNV | Intergenic | AD |
rs2114008 | chr4:133390458 | T>C | SNV | Intergenic | AD |
rs2114009 | chr4:133390311 | T>C | SNV | Intergenic | AD |
rs10894669 | chr11:133337045 | C>A | SNV | OPCML : Intron Variant | AD |
rs4379857 | chr11:133313709 | G>A / G>T | SNV | OPCML : Intron Variant | ND |
rs1941220 | chr11:133284546 | A>G | SNV | OPCML : Intron Variant | AD |
rs657152 | chr9:133263862 | A>C / A>T | SNV | ABO : Intron Variant | AD |
rs11936591 | chr4:133233577 | C>T | SNV | Intergenic | AD |
rs10935045 | chr3:133081302 | C>A | SNV | TMEM108 : Intron Variant | AD |
rs1541331 | chr9:133050630 | A>G | SNV | GTF3C5 : Intron Variant MIR6877 : 2KB Upstream Variant | AD |
rs11223321 | chr11:133013102 | A>C | SNV | OPCML : Intron Variant | AD |
rs2369955 | chr3:132974744 | A>C | SNV | Intergenic | AD |
rs12677246 | chr8:132955150 | C>G | SNV | TG : Intron Variant | AD |
rs10956683 | chr8:132819238 | G>A | SNV | PHF20L1 : Intron Variant | AD |
rs1793257 | chr11:132714224 | C>A / C>T | SNV | OPCML : Intron Variant | AD |
rs243446 | chrX:132694662 | A>G | SNV | HS6ST2 : Intron Variant | AD |
rs4936173 | chr11:132622531 | C>T | SNV | OPCML : Intron Variant | AD |
rs2842891 | chr6:132496758 | C>T | SNV | STX7 : Intron Variant | AD |
rs274551 | chr5:132391988 | T>C | SNV | SLC22A5 : Intron Variant | ND |
rs17689550 | chr5:132387373 | C>T | SNV | SLC22A5 : Intron Variant | AD |
rs11739484 | chr5:132321067 | A>G | SNV | SLC22A4 : Intron Variant LOC553103 : Intron Variant | AD |
rs6903616 | chr6:132296330 | C>T | SNV | MOXD1 : 3 Prime UTR Variant | AD |
rs17061146 | chr6:132292659 | C>T | SNV | Intergenic | AD |
rs11760080 | chr6:132286657 | G>A | SNV | Intergenic | AD |
rs2092236 | chr6:132285899 | A>G | SNV | Intergenic | AD |
rs1883339 | chr6:132279845 | G>A | SNV | Intergenic | AD |
rs924949 | chr3:132265544 | G>A | SNV | CPNE4 : Intron Variant | AD |
rs2274853 | chr9:132238978 | G>A / G>C | SNV | NTNG2 : Intron Variant | AD |
rs1868534 | chr11:132224572 | T>G | SNV | NTM : Intron Variant | ND |
rs6946056 | chr7:132185838 | A>C | SNV | PLXNA4 : Intron Variant | AD |
rs6968634 | chr7:132183083 | G>A | SNV | PLXNA4 : Intron Variant | AD |
rs896170 | chr7:132180333 | T>C | SNV | PLXNA4 : Intron Variant | AD |
rs3734989 | chr7:132179832 | T>C | SNV | PLXNA4 : Synonymous Variant | AD |
rs7808586 | chr7:132174737 | G>A / G>C | SNV | PLXNA4 : Intron Variant | AD |
rs10277421 | chr7:132174318 | T>C | SNV | PLXNA4 : Intron Variant | AD |
rs1991718 | chr8:132149077 | C>T | SNV | KCNQ3 : Intron Variant | AD |
rs1595411 | chr8:132147178 | G>A | SNV | KCNQ3 : Intron Variant | AD |
rs2469518 | chr8:132144220 | G>A | SNV | KCNQ3 : Intron Variant | AD |
rs10273901 | chr7:132143808 | T>C | SNV | PLXNA4 : Intron Variant | AD |
rs12634678 | chr3:132056472 | T>G | SNV | CPNE4 : Intron Variant LOC105374111 : Intron Variant | AD |
rs471677 | chr11:131957812 | A>C | SNV | NTM : Intron Variant | AD |
rs501050 | chr11:131939677 | C>T | SNV | NTM : Intron Variant | ND |
rs7768555 | chr6:131847222 | G>A | SNV | ENPP1 : Intron Variant | ND |
rs12340210 | chr9:131758437 | C>T | SNV | Intergenic | AD |
rs1041264 | chr9:131741953 | C>T | SNV | RAPGEF1 : 2KB Upstream Variant | AD |
rs10120010 | chr9:131685810 | C>T | SNV | RAPGEF1 : Intron Variant | AD |
rs12832187 | chr12:131669648 | C>T | SNV | Intergenic | AD |
rs2909678 | chr7:131649242 | T>C | SNV | Intergenic | AD |
rs17148121 | chr9:131628423 | C>T | SNV | RAPGEF1 : Intron Variant | AD |
rs10902443 | chr12:131566145 | G>A | SNV | Intergenic | ND |
rs13275290 | chr8:131554907 | G>A | SNV | Intergenic | AD |
rs7807320 | chr7:131542152 | G>T | SNV | PODXL : Intron Variant | AD |
rs6953894 | chr7:131538418 | A>G | SNV | PODXL : Intron Variant | AD |
rs12255578 | chr10:131144344 | G>T | SNV | TCERG1L : Intron Variant | ND |
rs3902786 | chr10:131083585 | A>T | SNV | Intergenic | AD |
rs4937598 | chr11:131064722 | G>A | SNV | Intergenic | AD |
rs58477043 | chr9:131051366-131051382 | delT / dupT / dupTT / dupTTT | Indel | LAMC3 : Intron Variant | AD |
rs4759814 | chr12:130970676 | T>G | SNV | ADGRD1 : Intron Variant | AD |
rs4759802 | chr12:130922632 | A>G / A>T | SNV | Intergenic | ND |
rs1655129 | chr10:130895898 | A>G | SNV | Intergenic | ND |
rs1655124 | chr10:130893462 | G>A | SNV | Intergenic | ND |
rs272146 | chr2:130780160 | C>A | SNV | POTEI : Intron Variant | AD |
rs17059529 | chr6:130768967 | G>A | SNV | LOC105378003 : Intron Variant | AD |
rs10505560 | chr8:130732742 | T>C | SNV | Intergenic | AD |
rs10848190 | chr12:130717490 | C>T | SNV | RIMBP2 : 2KB Upstream Variant | AD |
rs7958924 | chr12:130677635 | A>C | SNV | RIMBP2 : Intron Variant | CD |
rs11244096 | chr9:130675957 | G>A | SNV | PRDM12 : Intron Variant | ND |
rs2020202 | chr6:130663800 | T>C | SNV | Intergenic | AD |
rs9492684 | chr6:130647858 | A>C | SNV | Intergenic | ND |
rs16911018 | chr10:130632855 | G>A / G>T | SNV | Intergenic | AD |
rs2048779 | chr12:130497072 | A>C | SNV | RIMBP2 : Intron Variant | AD |
rs12210827 | chr6:130485171 | A>T | SNV | Intergenic | AD |
rs74676837 | chr8:130446408 | A>G | SNV | Intergenic | CD |
rs10956525 | chr8:130430605 | T>C | SNV | ASAP1 : Intron Variant | AD |
rs112765450 | chr8:130424403 | G>A | SNV | ASAP1 : Intron Variant | CD |
rs11060883 | chr12:130419855 | A>G | SNV | RIMBP2 : Intron Variant | ND |
rs7933236 | chr11:130241833 | G>C | SNV | ZBTB44 : Intron Variant | ND |
rs858723 | chr11:130224731 | C>T | SNV | Intergenic | ND |
rs10741210 | chr10:130186048 | G>A | SNV | Intergenic | AD |
rs10223341 | chr6:130174738 | G>T | SNV | SAMD3 : Intron Variant | OD |
rs7004884 | chr8:130123023 | A>G | SNV | ASAP1 : Intron Variant | AD |
rs11933661 | chr4:130091985 | C>T | SNV | Intergenic | AD |
rs6534762 | chr4:130057834 | A>G | SNV | Intergenic | AD |
rs1567193 | chr4:130041108 | T>C | SNV | Intergenic | AD |
rs942950 | chr10:130017410 | T>A / T>C | SNV | Intergenic | AD |
rs1993757 | chr12:129989920 | C>T | SNV | Intergenic | AD |
rs7099076 | chr10:129974707 | T>C | SNV | Intergenic | AD |
rs7858348 | chr9:129855609 | G>A | SNV | USP20 : Intron Variant | AD |
rs6912805 | chr6:129834568 | T>C | SNV | TMEM244 : Intron Variant | AD |
rs9492393 | chr6:129833522 | T>C | SNV | TMEM244 : Missense Variant | AD |
rs2707653 | chr2:129805369 | C>T | SNV | LOC107985945 : Intron Variant | AD |
rs2464786 | chr2:129792562 | G>A | SNV | LOC107985945 : Intron Variant | AD |
rs4837408 | chr9:129751861 | C>T | SNV | PTGES : Intron Variant | ND |
rs7979367 | chr12:129745862 | G>T | SNV | TMEM132D : Intron Variant | AD |
rs10819563 | chr9:129742923 | A>G | SNV | PTGES : Intron Variant | ND |
rs10829622 | chr10:129721248 | T>C | SNV | MGMT : Intron Variant LOC105378560 : Non Coding Transcript Variant | AD |
rs4751115 | chr10:129712029 | T>C | SNV | MGMT : Intron Variant LOC105378560 : Non Coding Transcript Variant | AD |
rs12213388 | chr6:129711600 | T>C | SNV | ARHGAP18 : 2KB Upstream Variant | AD |
rs16999497 | chrX:129601222 | T>C | SNV | Intergenic | AD |
rs10988439 | chr9:129589940 | G>T | SNV | Intergenic | AD |
rs10457526 | chr6:129575356 | G>T | SNV | Intergenic | AD |
rs2571577 | chr6:129476939 | T>C | SNV | LAMA2 : Intron Variant | AD |
rs17049483 | chr2:129444413 | C>T | SNV | LOC105373613 : Intron Variant | ND |
rs1433375 | chr4:129416904 | T>C | SNV | Intergenic | AD |
rs4837362 | chr9:129400975 | A>C / A>T | SNV | Intergenic | AD |
rs11060247 | chr12:129319609 | C>G / C>T | SNV | TMEM132D : Intron Variant | AD |
rs837899 | chr2:129266460 | G>A | SNV | LOC151121 : Intron Variant | AD |
rs6756671 | chr2:129249602 | G>A | SNV | LOC105373612 : Intron Variant LOC151121 : Intron Variant | AD |
rs837827 | chr2:129246578 | G>A | SNV | LOC105373612 : Intron Variant LOC151121 : Intron Variant | AD |
rs1251179 | chr2:129246162 | A>G | SNV | LOC105373612 : Intron Variant LOC151121 : Intron Variant | AD |
rs1441142 | chr2:129245705 | G>A | SNV | LOC105373612 : Intron Variant LOC151121 : Intron Variant | AD |
rs6708498 | chr2:129244613 | C>T | SNV | LOC105373612 : Non Coding Transcript Variant LOC151121 : Intron Variant | AD |
rs1441141 | chr2:129244500 | A>G | SNV | LOC105373612 : Non Coding Transcript Variant LOC151121 : Intron Variant | AD |
rs10167178 | chr2:129244152 | C>T | SNV | LOC151121 : Non Coding Transcript Variant LOC105373612 : 2KB Upstream Variant | AD |
rs4662641 | chr2:129242699 | G>A | SNV | LOC151121 : Non Coding Transcript Variant LOC105373612 : 2KB Upstream Variant | AD |
rs4662640 | chr2:129242223 | A>C | SNV | LOC151121 : Non Coding Transcript Variant | AD |
rs1251172 | chr2:129241617 | G>A | SNV | Intergenic | AD |
rs2952621 | chr2:129240870 | T>C | SNV | Intergenic | AD |
rs935085 | chr2:129240460 | T>C | SNV | Intergenic | AD |
rs894110 | chr2:129239970 | C>A / C>G | SNV | Intergenic | AD |
rs3856372 | chr2:129239510 | T>A | SNV | Intergenic | AD |
rs1734330 | chr2:129239415 | A>T | SNV | Intergenic | AD |
rs879533 | chr2:129239173 | T>A | SNV | Intergenic | AD |
rs35878075 | chr2:129237928 | G>A | SNV | Intergenic | AD |
rs1660895 | chr2:129236759 | A>T | SNV | Intergenic | AD |
rs1078826 | chr2:129233439 | G>A | SNV | Intergenic | AD |
rs13033217 | chr2:129233296 | T>C | SNV | Intergenic | AD |
rs4662907 | chr2:129232624 | G>A | SNV | Intergenic | AD |
rs12472824 | chr2:129232274 | C>T | SNV | Intergenic | AD |
rs1251205 | chr2:129229947 | T>A | SNV | Intergenic | AD |
rs2406641 | chr2:129227852 | A>G | SNV | Intergenic | AD |
rs1251216 | chr2:129227637 | G>C | SNV | Intergenic | AD |
rs1268546 | chr2:129227609 | T>C | SNV | Intergenic | AD |
rs1251215 | chr2:129227581 | C>T | SNV | Intergenic | AD |
rs1251214 | chr2:129227541 | C>A / C>G | SNV | Intergenic | AD |
rs735987 | chr2:129226829 | G>A | SNV | Intergenic | AD |
rs1270481 | chr2:129226091 | T>C | SNV | Intergenic | AD |
rs1251210 | chr2:129225968 | G>A | SNV | Intergenic | AD |
rs2119515 | chr2:129225558 | G>A / G>T | SNV | Intergenic | AD |
rs1251209 | chr2:129225441 | A>G / A>T | SNV | Intergenic | AD |
rs13033188 | chr2:129225383 | C>T | SNV | Intergenic | AD |
rs1757939 | chr4:129225021 | T>C | SNV | Intergenic | CD |
rs1251207 | chr2:129224299 | G>T | SNV | Intergenic | AD |
rs4895846 | chr6:129063222 | T>C | SNV | LAMA2 : Intron Variant | AD |
rs11682667 | chr2:129061896 | T>C | SNV | Intergenic | AD |
rs4534007 | chr6:129052544 | G>A | SNV | LAMA2 : Intron Variant | AD |
rs729302 | chr7:128928906 | A>C | SNV | Intergenic | AD |
rs6486717 | chr12:128683327 | T>G | SNV | TMEM132C : Intron Variant | AD |
rs1489430 | chr12:128681600 | T>C | SNV | TMEM132C : Intron Variant | AD |
rs10773566 | chr12:128679103 | G>T | SNV | TMEM132C : Intron Variant | AD |
rs11608979 | chr12:128677080 | G>A | SNV | TMEM132C : Intron Variant | AD |
rs7960753 | chr12:128673822 | A>C | SNV | TMEM132C : Intron Variant | AD |
rs17056140 | chr6:128630162 | T>C | SNV | Intergenic | AD |
rs10230965 | chr7:128582912 | G>T | SNV | LOC101928451 : Intron Variant | AD |
rs6923822 | chr6:128518325 | G>A / G>C | SNV | PTPRK : Intron Variant | AD |
rs10808570 | chr8:128451289 | A>C | SNV | LINC00824 : Intron Variant | AD |
rs1651939 | chr7:128374082 | C>A | SNV | Intergenic | AD |
rs2999090 | chr3:128212497 | G>A | SNV | EEFSEC : Intron Variant | AD |
rs1785039 | chr11:128030684 | A>G | SNV | Intergenic | AD |
rs4837223 | chr9:128014128 | C>T | SNV | Intergenic | AD |
rs10496665 | chr2:127910983 | A>G | SNV | Intergenic | AD |
rs1525855 | chr3:127829636 | G>A | SNV | Intergenic | AD |
rs2099269 | chr12:127775035 | G>T | SNV | Intergenic | AD |
rs2594210 | chr3:127543914 | G>A | SNV | LOC107986125 : Non Coding Transcript Variant | AD |
rs1512454 | chr6:127529821 | G>A | SNV | Intergenic | AD |
rs17012484 | chr4:127520412 | A>C | SNV | Intergenic | ND |
rs11018077 | chr10:127429224 | G>A | SNV | DOCK1 : Intron Variant | AD |
rs10847282 | chr12:127145439 | C>T | SNV | LOC107984450 : Non Coding Transcript Variant LOC107984449 : Intron Variant | AD |
rs1137845 | chr2:127063631 | G>A | SNV | BIN1 : Synonymous Variant | AD |
rs2237781 | chr7:127034996 | G>A | SNV | GRM8 : Intron Variant | ND |
rs10256873 | chr7:126728238 | G>A / G>C | SNV | GRM8 : Intron Variant | AD |
rs7590496 | chr2:126600111 | C>A | SNV | LOC105373602 : Non Coding Transcript Variant | AD |
rs1687482 | chr3:126496851 | T>G | SNV | UROC1 : Intron Variant | AD |
rs4870976 | chr8:126466080 | G>A | SNV | Intergenic | AD |
rs4388209 | chr5:126422681 | T>C | SNV | GRAMD3 : Intron Variant | AD |
rs2253162 | chr8:126322765 | A>G / A>T | SNV | Intergenic | AD |
rs10794077 | chr10:126282489 | G>A | SNV | ADAM12 : Intron Variant | ND |
rs11924509 | chr3:126215378 | G>A | SNV | LOC105374086 : Non Coding Transcript Variant | AD |
rs13082246 | chr3:126192112 | G>A | SNV | ALDH1L1-AS2 : Intron Variant | AD |
rs9874508 | chr3:126183574 | G>A | SNV | ALDH1L1-AS2 : Intron Variant | AD |
rs7617733 | chr3:126171901 | G>A | SNV | ALDH1L1 : Intron Variant | AD |
rs10847023 | chr12:125959974 | T>C | SNV | LINC00939 : Intron Variant | AD |
rs6804367 | chr3:125921068 | C>T | SNV | FAM86JP : Intron Variant | CD |
rs1558062 | chr12:125768961 | G>A | SNV | Intergenic | AD |
rs402608 | chr7:125699264 | A>G | SNV | Intergenic | AD |
rs1490996 | chr5:125610839 | A>G | SNV | LOC105379160 : Intron Variant | AD |
rs7829236 | chr8:125558035 | G>A | SNV | LOC105375746 : Intron Variant | AD |
rs1934990 | chr6:125345675 | C>A | SNV | LOC107986640 : 2KB Upstream Variant | AD |
rs12284594 | chr11:125309957 | A>G / A>T | SNV | PKNOX2 : Intron Variant | AD |
rs10893366 | chr11:125308507 | C>T | SNV | PKNOX2 : Intron Variant | AD | ND |
rs10893365 | chr11:125306541 | T>C | SNV | PKNOX2 : Intron Variant | AD |
rs750338 | chr11:125302697 | A>G | SNV | PKNOX2 : Intron Variant | AD | ND |
rs11602925 | chr11:125301535 | A>G | SNV | PKNOX2 : Intron Variant | AD |
rs11220015 | chr11:125301478 | G>A | SNV | PKNOX2 : Intron Variant | AD |
rs1426153 | chr11:125300743 | A>G | SNV | PKNOX2 : Intron Variant | AD | ND |
rs7008482 | chr8:125255388 | T>G | SNV | NSMCE2 : Intron Variant | AD |
rs9285980 | chr10:125225933 | T>C | SNV | Intergenic | AD |
rs6895323 | chr5:125193762 | G>C | SNV | LOC101927421 : Intron Variant | CD |
rs55644503 | chr5:125190620 | T>C | SNV | LOC101927421 : Intron Variant | ND |
rs6763338 | chr3:125168389 | C>A | SNV | SLC12A8 : Intron Variant | ND |
rs601813 | chr11:125136457 | A>G | SNV | PKNOX2 : Intron Variant | AD |
rs585977 | chr11:125131947 | G>A | SNV | PKNOX2 : Intron Variant | AD |
rs597900 | chr11:125127625 | C>T | SNV | PKNOX2 : Intron Variant | AD |
rs10893332 | chr11:125125208 | C>T | SNV | PKNOX2 : Intron Variant | AD |
rs2390798 | chr4:125086041 | G>A | SNV | Intergenic | AD |
rs12761801 | chr10:125084412 | C>T | SNV | CTBP2 : Intron Variant | ND |
rs571846 | chr6:125080418 | C>T | SNV | RNF217 : Intron Variant | AD |
rs11595908 | chr10:125018107 | C>T | SNV | CTBP2 : Intron Variant | AD |
rs12781214 | chr10:125013480 | C>T | SNV | CTBP2 : Intron Variant | AD |
rs9321013 | chr6:125009775 | G>A | SNV | RNF217 : Intron Variant | ND |
rs4962416 | chr10:125008303 | T>C | SNV | CTBP2 : Intron Variant | AD |
rs11596226 | chr10:124986796 | T>G | SNV | ZRANB1 : 3 Prime UTR Variant | AD |
rs4580006 | chr12:124976121 | T>A | SNV | DHX37 : Intron Variant | AD |
rs7373878 | chr3:124891391 | G>T | SNV | ITGB5 : Intron Variant | AD |
rs6771896 | chr3:124826903 | G>A | SNV | ITGB5 : Intron Variant | AD |
rs16900003 | chr8:124751642 | G>A | SNV | Intergenic | AD |
rs2629540 | chr10:124737579 | G>C | SNV | FAM53B : Intron Variant | CD |
rs11057750 | chr12:124674216 | A>G | SNV | Intergenic | AD |
rs3781452 | chr10:124666560 | C>T | SNV | FAM53B : Intron Variant | AD |
rs3781458 | chr10:124655362 | C>T | SNV | FAM53B : Intron Variant | AD |
rs17152064 | chr10:124579190 | C>T | SNV | LHPP : Intron Variant | ND |
rs6438847 | chr3:124578798 | A>C | SNV | KALRN : Intron Variant LOC105374076 : 2KB Upstream Variant | AD |
rs9327332 | chr5:124553888 | A>C | SNV | Intergenic | AD |
rs10061885 | chr5:124552638 | C>T | SNV | Intergenic | AD |
rs34997829 | chr10:124546821 | G>C | SNV | LHPP : Intron Variant | AD |
rs150954431 | chr12:124517777 | C>T | SNV | NCOR2 : Intron Variant | CD |
rs555540 | chr3:124448118 | G>A / G>T | SNV | KALRN : Intron Variant | AD |
rs13239910 | chr7:124438555 | T>C / T>G | SNV | Intergenic | AD |
rs192590503 | chr6:124215869 | G>A | SNV | NKAIN2 : Intron Variant | OD |
rs10846616 | chr12:124176393 | A>C | SNV | ZNF664-FAM101A : Intron Variant | AD |
rs594664 | chr6:124121141 | C>T | SNV | NKAIN2 : Intron Variant | ND |
rs526257 | chr11:124092093 | G>A | SNV | Intergenic | ND |
rs638299 | chr11:124085688 | A>C | SNV | LOC105369545 : Intron Variant | ND |
rs488582 | chr11:124084918 | T>C | SNV | LOC105369545 : Intron Variant | ND |
rs7448080 | chr5:124062405 | T>C | SNV | LINC01170 : Intron Variant | AD |
rs330438 | chr5:123977527 | C>A | SNV | Intergenic | AD |
rs4678073 | chr3:123948677 | A>C / A>T | SNV | CCDC14 : Intron Variant | AD |
rs10511417 | chr3:123816489 | T>C | SNV | MYLK : Intron Variant | AD |
rs17256536 | chr8:123686935 | A>G | SNV | ANXA13 : Intron Variant | AD |
rs2589839 | chr4:123670981 | T>C | SNV | LINC01091 : Intron Variant | AD |
rs979537 | chr6:123661921 | T>C | SNV | LOC105377981 : Intron Variant | AD |
rs1579036 | chr5:123585409 | G>A | SNV | CSNK1G3 : Intron Variant | ND |
rs6813400 | chr4:123562157 | A>C | SNV | Intergenic | AD |
rs4076851 | chr4:123556545 | G>A | SNV | Intergenic | AD |
rs199732820 | chrX:123529690 | C>T | SNV | Intergenic | ND |
rs845104 | chr10:123423467 | A>T | SNV | LOC105378531 : Non Coding Transcript Variant | ND |
rs12773354 | chr10:123234424 | C>T | SNV | Intergenic | AD |
rs12559898 | chrX:123197971 | G>A | SNV | GRIA3 : Intron Variant | ND |
rs10794595 | chr10:123121986 | T>C | SNV | Intergenic | ND |
rs3013029 | chrX:123008072 | A>G | SNV | Intergenic | AD |
rs4871326 | chr8:122930907 | T>C | SNV | ZHX2 : Intron Variant | ND |
rs17653439 | chr10:122930775 | G>A | SNV | C10orf88 : 500B Downstream Variant | AD |
rs6470120 | chr8:122868979 | G>A | SNV | ZHX2 : Intron Variant | AD | ND |
rs997795 | chr8:122760595 | T>G | SNV | Intergenic | AD |
rs10985760 | chr9:122750491 | T>C / T>G | SNV | OR1L6 : Missense Variant | ND |
rs13400652 | chr2:122638301 | C>T | SNV | Intergenic | ND |
rs10739616 | chr9:122622509 | A>G | SNV | OR1B1 : Intron Variant | AD |
rs1329957 | chr9:122615226 | A>G | SNV | OR1Q1 : Missense Variant OR1B1 : Intron Variant | AD |
rs7925049 | chr11:122581485 | A>G | SNV | Intergenic | AD |
rs4836019 | chr5:122517722 | A>T | SNV | Intergenic | AD |
rs4835803 | chr5:122516836 | C>T | SNV | Intergenic | AD |
rs2002594 | chr3:122392714 | A>G | SNV | FAM162A : Intron Variant | AD |
rs11200559 | chr10:122337912 | G>T | SNV | BTBD16 : Intron Variant | AD |
rs7042018 | chr9:122241249 | A>G | SNV | RBM18 : Non Coding Transcript Variant | AD |
rs10733657 | chr9:122239706 | C>T | SNV | RBM18 : Non Coding Transcript Variant | AD |
rs13356385 | chr5:122234922 | G>A | SNV | Intergenic | AD |
rs492085 | chr11:122123992 | G>T | SNV | MIR100HG : Intron Variant | AD |
rs1922179 | chr2:122089563 | C>T | SNV | LOC105373592 : Intron Variant | AD |
rs16911292 | chr9:122019270 | C>A / C>T | SNV | TTLL11 : Intron Variant | ND |
rs1465040 | chr4:122007101 | T>C | SNV | Intergenic | OD |
rs4496732 | chr5:121982225 | C>T | SNV | SRFBP1 : Intron Variant | ND |
rs6838639 | chr4:121978010 | G>A | SNV | LOC102724158 : Intron Variant | AD |
rs1448130 | chr11:121944715 | G>A | SNV | Intergenic | AD |
rs747915 | chr11:121908956 | T>C | SNV | Intergenic | AD |
rs2230681 | chr12:121888906 | T>C | SNV | PSMD9 : Missense Variant HPD : 2KB Upstream Variant | ND |
rs17148568 | chr5:121854755 | A>C | SNV | LOC105379149 : Intron Variant | AD |
rs9826473 | chr3:121837372 | C>T | SNV | EAF2 : Intron Variant | AD |
rs4413346 | chr3:121767463 | T>C | SNV | Intergenic | AD |
rs17337279 | chr11:121697408 | C>T | SNV | Intergenic | AD |
rs9297647 | chr8:121671200 | A>G | SNV | LOC105375732 : Intron Variant | AD |
rs10227063 | chr7:121635423 | A>G | SNV | Intergenic | AD |
rs10253361 | chr7:121635175 | C>T | SNV | Intergenic | AD |
rs1757321 | chr9:121569480 | C>T | SNV | DAB2IP : Intron Variant LOC107987016 : Non Coding Transcript Variant | AD |
rs10213966 | chr5:121461456 | A>G | SNV | Intergenic | AD |
rs1469447 | chr5:121454833 | C>A | SNV | Intergenic | AD |
rs10463741 | chr5:121444191 | A>G | SNV | Intergenic | AD |
rs10065963 | chr5:121441072 | C>T | SNV | Intergenic | AD |
rs523815 | chr4:121379140 | G>A | SNV | QRFPR : Intron Variant | AD |
rs4936618 | chr11:121353287 | A>C | SNV | Intergenic | AD |
rs798949 | chr7:121125900 | T>A / T>C | SNV | CPED1 : Intron Variant | AD |
rs10886848 | chr10:121081757 | C>A / C>T | SNV | Intergenic | ND |
rs3751151 | chr12:121004396 | T>A | SNV | C12orf43 : Synonymous Variant | AD |
rs12491742 | chr3:120971356 | T>G | SNV | STXBP5L : Intron Variant | AD |
rs939144 | chr8:120967417 | G>A | SNV | Intergenic | AD |
rs7303401 | chr12:120966253 | T>A | SNV | Intergenic | AD |
rs6988609 | chr8:120959818 | A>C | SNV | Intergenic | AD |
rs7824584 | chr8:120958799 | T>C | SNV | Intergenic | AD |
rs10505382 | chr8:120916129 | T>G | SNV | Intergenic | ND |
rs7103228 | chr11:120710058 | G>A / G>T | SNV | GRIK4 : Intron Variant | ND |
rs11217974 | chr11:120691780 | A>G | SNV | GRIK4 : Intron Variant | ND |
rs7741833 | chr6:120679901 | A>G | SNV | Intergenic | AD |
rs728115 | chr7:120665095 | G>A | SNV | KCND2 : Intron Variant | ND |
rs11780390 | chr8:120637885 | G>A | SNV | SNTB1 : Intron Variant | AD |
rs7613732 | chr3:120631658 | A>G | SNV | HGD : Intron Variant | AD |
rs4833652 | chr4:120553417 | A>G | SNV | Intergenic | ND |
rs300974 | chr5:120534068 | G>A | SNV | PRR16 : Intron Variant | AD |
rs10477601 | chr5:120447866 | G>A | SNV | LOC105379145 : Intron Variant | AD |
rs13171094 | chr5:120447451 | A>G / A>T | SNV | LOC105379145 : Intron Variant | AD |
rs17245504 | chr11:120308044 | T>G | SNV | POU2F3 : Intron Variant | ND |
rs4142654 | chr11:120296348 | A>G | SNV | POU2F3 : Intron Variant | AD |
rs11603757 | chr11:120293949 | G>T | SNV | POU2F3 : Intron Variant | ND |
rs6589804 | chr11:120290932 | G>A | SNV | POU2F3 : Intron Variant LOC105369531 : Non Coding Transcript Variant | ND |
rs3931840 | chr2:120283771 | A>C | SNV | RALB : Intron Variant | AD |
rs12857770 | chrX:120259745 | C>T | SNV | TMEM255A : Non Coding Transcript Variant | AD |
rs1370379 | chr2:120257013 | C>T | SNV | RALB : Intron Variant | AD |
rs3980213 | chr2:120247403 | A>G | SNV | RALB : Intron Variant LOC105373583 : 2KB Upstream Variant | AD |
rs155155 | chr6:120169190 | A>G | SNV | Intergenic | AD |
rs17081960 | chr6:120163633 | C>T | SNV | Intergenic | AD |
rs12661222 | chr6:120131483 | A>G | SNV | Intergenic | AD |
rs9649948 | chr8:119901295 | T>C | SNV | DEPTOR : Intron Variant | CD |
rs203339 | chr12:119798950 | T>C | SNV | CIT : Intron Variant | AD |
rs454510 | chr1:119652419 | A>G | SNV | Intergenic | AD |
rs196335 | chr10:119652349 | C>T | SNV | BAG3 : Intron Variant | AD |
rs1346520 | chr5:119650293 | G>A / G>C | SNV | Intergenic | AD |
rs12109691 | chr5:119630805 | G>A | SNV | FAM170A : Intron Variant | AD |
rs196313 | chr10:119623524 | G>A | SNV | Intergenic | AD |
rs184497 | chr5:119617824 | T>C | SNV | Intergenic | AD |
rs10886486 | chr10:119459060 | A>C | SNV | Intergenic | AD |
rs11198934 | chr10:119458171 | C>T | SNV | Intergenic | AD |
rs1999628 | chr10:119457549 | T>A | SNV | Intergenic | AD |
rs1999627 | chr10:119457411 | G>A | SNV | Intergenic | AD |
rs2297641 | chr10:119452893 | C>T | SNV | GRK5 : Intron Variant | AD |
rs1316543 | chr10:119445148 | G>A | SNV | GRK5 : Intron Variant | AD |
rs9372532 | chr6:119408545 | T>C | SNV | Intergenic | AD |
rs170099 | chr7:119360158 | C>T | SNV | Intergenic | AD |
rs838530 | chr1:119354876 | T>C | SNV | LOC105378934 : Intron Variant | AD |
rs838532 | chr1:119354204 | T>C | SNV | LOC105378934 : Intron Variant | AD |
rs3813301 | chr5:119339551 | A>G | SNV | TNFAIP8 : Intron Variant | ND |
rs17164572 | chr5:119338002 | C>T | SNV | TNFAIP8 : Intron Variant | ND |
rs7704398 | chr5:119331947 | C>T | SNV | TNFAIP8 : Intron Variant | ND |
rs699771 | chr1:119329354 | C>T | SNV | LOC105378934 : Intron Variant | AD | ND |
rs1891224 | chr1:119312119 | G>A | SNV | Intergenic | AD |
rs72840936 | chr2:119266116 | G>C | SNV | STEAP3 : 500B Downstream Variant LOC105373581 : Non Coding Transcript Variant | CD |
rs7095989 | chr10:119265585 | A>C | SNV | GRK5 : Intron Variant | AD |
rs1341797 | chr1:119252510 | G>A | SNV | LOC101929147 : Intron Variant LOC107985192 : Intron Variant | AD |
rs17080911 | chr6:119248936 | C>A | SNV | MAN1A1 : Intron Variant | AD |
rs17805141 | chr2:119247993 | C>T | SNV | STEAP3 : Synonymous Variant STEAP3-AS1 : Intron Variant | CD |
rs4849770 | chr2:119199450 | G>A / G>C | SNV | LOC107985941 : Intron Variant | AD |
rs10886416 | chr10:119193162 | C>A | SNV | Intergenic | AD |
rs11123504 | chr2:119185310 | G>A | SNV | LOC107985941 : Intron Variant | AD |
rs6758051 | chr2:119156525 | T>G | SNV | C1QL2 : 3 Prime UTR Variant | CD |
rs745888 | chr2:119152738 | C>T | SNV | Intergenic | CD |
rs745884 | chr2:119151809 | C>A / C>G / C>T | SNV | Intergenic | CD |
rs13020121 | chr2:119147377 | G>A | SNV | Intergenic | CD |
rs7597287 | chr2:119146393 | G>C | SNV | Intergenic | CD |
rs7717384 | chr5:119145510 | G>A | SNV | DMXL1 : Intron Variant | AD |
rs4531480 | chr11:119072889 | T>C | SNV | VPS11 : Intron Variant | AD |
rs17261061 | chrX:119055458 | C>A | SNV | Intergenic | AD |
rs4730908 | chr7:119017956 | C>G | SNV | Intergenic | AD |
rs4295599 | chr7:118997601 | A>C | SNV | Intergenic | AD |
rs6466686 | chr7:118996763 | C>T | SNV | Intergenic | AD |
rs7812233 | chr7:118978108 | G>A | SNV | Intergenic | AD |
rs4518581 | chr7:118970601 | G>A | SNV | Intergenic | AD |
rs10923714 | chr1:118970290 | G>A | SNV | TBX15 : Intron Variant | AD |
rs10953885 | chr7:118968349 | T>C | SNV | Intergenic | AD |
rs10953881 | chr7:118968071 | C>T | SNV | Intergenic | AD |
rs4268066 | chr7:118961051 | C>T | SNV | Intergenic | AD |
rs10281955 | chr7:118944637 | G>A | SNV | Intergenic | AD |
rs4834729 | chr4:118943912 | C>T | SNV | SYNPO2 : Intron Variant | AD |
rs10249276 | chr7:118938630 | A>G | SNV | Intergenic | AD |
rs7905194 | chr10:118938179 | C>T | SNV | Intergenic | AD |
rs665648 | chr11:118894574 | G>A | SNV | CXCR5 : Missense Variant | AD |
rs4767725 | chr12:118831166 | C>T | SNV | LOC105370016 : Intron Variant LOC107984472 : Intron Variant | AD |
rs17144687 | chr5:118824240 | A>C | SNV | Intergenic | AD |
rs1784300 | chr11:118808920 | A>T | SNV | Intergenic | ND |
rs10984229 | chr9:118797075 | T>C | SNV | Intergenic | AD |
rs1688609 | chr6:118713978 | G>T | SNV | Intergenic | AD |
rs4687935 | chr3:118694631 | G>A | SNV | LOC105374060 : Intron Variant LOC107983969 : Intron Variant | ND |
rs1520780 | chr12:118601920 | G>A | SNV | Intergenic | AD |
rs17642621 | chr4:118487196 | G>A | SNV | LOC105379403 : Intron Variant | AD |
rs7316050 | chr12:118458665 | A>T | SNV | Intergenic | AD |
rs577196 | chr3:118439050 | C>T | SNV | Intergenic | AD |
rs2166753 | chr3:118362178 | G>A / G>C | SNV | Intergenic | AD |
rs10923556 | chr1:118360573 | C>T | SNV | Intergenic | AD |
rs10802023 | chr1:118336033 | T>C | SNV | Intergenic | AD |
rs4375253 | chr1:118322345 | C>T | SNV | Intergenic | AD |
rs10864971 | chr2:118243076 | C>T | SNV | Intergenic | AD |
rs4267900 | chr5:118119334 | C>A | SNV | LOC102467224 : Intron Variant | ND |
rs3016863 | chr11:118037613 | A>G | SNV | TMPRSS4-AS1 : Intron Variant | AD |
rs5745879 | chr12:118029840 | C>A / C>T | SNV | RFC5 : Intron Variant | AD |
rs7777391 | chr7:117981823 | A>G | SNV | Intergenic | ND |
rs4142224 | chr2:117958614 | C>T | SNV | CCDC93 : Intron Variant | AD |
rs10113582 | chr8:117796654 | T>C | SNV | Intergenic | AD |
rs7303368 | chr12:117697134 | C>A / C>G / C>T | SNV | KSR2 : Intron Variant | AD |
rs553637 | chr11:117590887 | C>T | SNV | DSCAML1 : Intron Variant | AD |
rs2635190 | chr4:117512484 | C>T | SNV | LINC01378 : Intron Variant | AD |
rs16905611 | chr9:117419702 | A>C | SNV | Intergenic | ND |
rs12858772 | chrX:117353885 | C>T | SNV | Intergenic | AD |
rs2532812 | chr10:117292277 | G>A | SNV | PDZD8 : Intron Variant | AD |
rs363294 | chr10:117284043 | C>T | SNV | PDZD8 : Missense Variant | AD |
rs2293050 | chr12:117281017 | C>T | SNV | NOS1 : Intron Variant | AD |
rs12098035 | chr1:117216829 | C>T | SNV | Intergenic | AD |
rs1892409 | chr1:117216703 | C>T | SNV | Intergenic | AD |
rs3806373 | chr1:117211437 | T>C | SNV | VTCN1 : 2KB Upstream Variant | AD |
rs7736676 | chr5:117194234 | A>G | SNV | Intergenic | CD |
rs74335618 | chr7:117175543 | T>C | SNV | ST7 : Intron Variant | AD |
rs9844985 | chr3:117163885 | A>C | SNV | Intergenic | AD |
rs6490111 | chr12:117127476 | G>T | SNV | TESC-AS1 : Intron Variant | AD |
rs1875144 | chr12:117037373 | T>C | SNV | Intergenic | AD |
rs10502221 | chr11:116956154 | C>T | SNV | SIK3 : Intron Variant | AD |
rs4430250 | chrX:116954224 | C>T | SNV | Intergenic | AD |
rs13288277 | chr9:116947149 | A>G | SNV | ASTN2 : Intron Variant | AD |
rs720133 | chr8:116904042 | T>C | SNV | Intergenic | AD |
rs1536428 | chr9:116853763 | A>G | SNV | ASTN2 : Intron Variant | AD |
rs1326814 | chr9:116849749 | C>G / C>T | SNV | ASTN2 : Intron Variant LOC105376238 : Non Coding Transcript Variant | AD |
rs153585 | chr5:116846657 | G>T | SNV | Intergenic | ND |
rs6870730 | chr5:116825255 | G>A | SNV | Intergenic | AD |
rs7097645 | chr10:116800966 | A>G | SNV | HSPA12A : Intron Variant | AD |
rs7833054 | chr8:116668792 | A>G | SNV | EIF3H : Intron Variant | AD |
rs1401083 | chr3:116654960 | A>G | SNV | Intergenic | AD |
rs7649435 | chr3:116634685 | A>G | SNV | Intergenic | AD |
rs73012959 | chr11:116618927 | C>T | SNV | Intergenic | AD |
rs154576 | chr5:116525936 | G>A | SNV | SEMA6A : Intron Variant | AD |
rs4129295 | chr8:116463359 | A>C | SNV | LOC105375711 : Intron Variant | AD |
rs2252790 | chr6:116342160 | G>A | SNV | DSE : Intron Variant | AD |
rs10496515 | chr2:116313637 | T>C | SNV | LOC105373576 : Intron Variant | ND |
rs4938246 | chr11:116268402 | G>A | SNV | Intergenic | AD |
rs7128824 | chr11:116261235 | A>C | SNV | Intergenic | AD |
rs17473320 | chr11:116258300 | C>T | SNV | Intergenic | AD |
rs10891937 | chr11:116256087 | G>A | SNV | Intergenic | AD |
rs10891936 | chr11:116255743 | G>A / G>T | SNV | Intergenic | AD |
rs1009746 | chr11:116248195 | T>G | SNV | Intergenic | AD |
rs62271282 | chr3:116039221 | T>C / T>G | SNV | LSAMP : Intron Variant | AD |
rs16824395 | chr3:116021872 | A>G | SNV | LSAMP : Intron Variant | AD |
rs1529442 | chr5:116013678 | C>T | SNV | LVRN : Intron Variant | AD |
rs2615891 | chr10:115880805 | G>A | SNV | ATRNL1 : Intron Variant | ND |
rs10251693 | chr7:115643559 | T>C | SNV | Intergenic | CD |
rs2513630 | chr11:115573237 | G>A / G>T | SNV | Intergenic | AD |
rs10982769 | chr9:115492709 | T>C | SNV | Intergenic | AD |
rs1632812 | chr9:115461151 | G>A | SNV | Intergenic | AD |
rs6469576 | chr8:115307833 | G>A | SNV | Intergenic | AD |
rs10489530 | chr1:115297059 | G>A | SNV | NGF : Intron Variant | AD |
rs195204 | chr1:115191470 | T>C | SNV | Intergenic | AD |
rs195207 | chr1:115185327 | C>A | SNV | Intergenic | AD |
rs11581510 | chr1:115129524 | G>A / G>T | SNV | Intergenic | AD |
rs17479252 | chr1:115079239 | C>T | SNV | TSPAN2 : Intron Variant | AD |
rs11102878 | chr1:115048377 | T>C | SNV | TSPAN2 : 3 Prime UTR Variant | AD |
rs1998008 | chr1:115037919 | A>C | SNV | Intergenic | AD |
rs13150562 | chr4:115036437 | T>C | SNV | NDST4 : Intron Variant | AD |
rs1321108 | chr1:115029744 | A>G | SNV | TSHB : 2KB Upstream Variant | AD |
rs13237006 | chr7:115018432 | A>G | SNV | MDFIC : 3 Prime UTR Variant | AD |
rs360595 | chr1:114930585 | G>A | SNV | SYCP1 : Intron Variant | AD |
rs7113782 | chr11:114771901 | A>C | SNV | NXPE2 : Intron Variant | AD |
rs12108602 | chr4:114719413 | A>G | SNV | Intergenic | AD |
rs12705988 | chr7:114714947 | A>G | SNV | Intergenic | AD |
rs1359992 | chr9:114668331 | A>T | SNV | LOC100505478 : Missense Variant | AD |
rs10982289 | chr9:114552494 | G>A | SNV | Intergenic | AD |
rs5945988 | chrX:114484729 | G>A | SNV | Intergenic | AD |
rs2416371 | chr5:114440173 | C>T | SNV | KCNN2 : Intron Variant | AD |
rs4705665 | chr5:114407956 | A>G | SNV | KCNN2 : Intron Variant | AD |
rs1920597 | chr12:114266287 | G>A | SNV | Intergenic | AD |
rs549427 | chr11:114214137 | G>A | SNV | ZBTB16 : Intron Variant | ND |
rs7971457 | chr12:114178002 | T>C | SNV | Intergenic | AD |
rs10492333 | chr12:114137672 | T>C | SNV | Intergenic | AD |
rs529989 | chr1:114135326 | C>A | SNV | SYT6 : Intron Variant | ND |
rs1570589 | chr9:114112075 | A>G | SNV | Intergenic | AD |
rs2282237 | chr6:114057806 | C>T | SNV | HS3ST5 : Synonymous Variant LOC101927768 : Intron Variant | AD |
rs898078 | chr12:114025782 | G>A | SNV | LOC105369993 : Intron Variant | AD |
rs324556 | chr3:114012440 | G>T | SNV | CCDC191 : Intron Variant LOC105374048 : Intron Variant | AD |
rs17653713 | chr10:113986660 | C>A / C>T | SNV | Intergenic | AD |
rs3903132 | chr3:113981879 | T>C | SNV | ZDHHC23 : Intron Variant CCDC191 : Intron Variant | AD |
rs10513224 | chr9:113979159 | A>C | SNV | ZNF618 : Intron Variant | AD |
rs10012206 | chr4:113955964 | T>C | SNV | ARSJ : Intron Variant | AD |
rs2566980 | chr3:113841173 | A>C | SNV | GRAMD1C : Intron Variant | AD |
rs10567 | chr10:113834966 | C>T | SNV | DCLRE1A : 3 Prime UTR Variant | ND |
rs1482350 | chr5:113833723 | C>T | SNV | Intergenic | AD |
rs1116657 | chr5:113830440 | T>C | SNV | Intergenic | AD |
rs11196449 | chr10:113720823 | T>C | SNV | CASP7 : Intron Variant | AD |
rs3124743 | chr10:113704412 | A>G | SNV | CASP7 : Intron Variant | AD |
rs6533710 | chr4:113668110 | A>G | SNV | CAMK2D : Intron Variant | AD |
rs3121491 | chr10:113662237 | G>A | SNV | NRAP : Intron Variant | AD |
rs11066660 | chr12:113638849 | G>A | SNV | LOC105369990 : 2KB Upstream Variant | AD |
rs4918853 | chr10:113570371 | T>C | SNV | HABP2 : Intron Variant | AD |
rs11066595 | chr12:113544717 | C>G | SNV | Intergenic | AD |
rs35616138 | chr10:113460253 | A>G / A>T | SNV | LOC107984269 : Non Coding Transcript Variant | AD |
rs10891537 | chr11:113340648 | T>A / T>G | SNV | TTC12 : Intron Variant | AD |
rs10502172 | chr11:113328424 | C>T | SNV | TTC12 : Intron Variant | AD |
rs1191694 | chr2:113327259 | C>T | SNV | LOC101927400 : Intron Variant LOC105373567 : 2KB Upstream Variant | AD |
rs1191695 | chr2:113325786 | T>C | SNV | LOC101927400 : Intron Variant LOC105373567 : 2KB Upstream Variant | AD |
rs688011 | chr11:113283448 | G>A | SNV | LOC105369499 : Intron Variant | ND |
rs2288158 | chr11:113262954 | T>G | SNV | NCAM1 : Intron Variant | ND |
rs6996697 | chr8:113262046 | A>G | SNV | CSMD3 : Intron Variant | AD |
rs10505201 | chr8:113214414 | G>A | SNV | CSMD3 : Intron Variant | AD |
rs6753019 | chr2:113190582 | G>A | SNV | PSD4 : Intron Variant | AD |
rs28463004 | chr11:113156036 | A>G | SNV | NCAM1 : Intron Variant | CD |
rs4979215 | chr9:113141849 | C>T | SNV | Intergenic | AD |
rs1881942 | chr3:113133204 | T>C | SNV | Intergenic | ND |
rs7867889 | chr9:113131960 | G>A | SNV | Intergenic | AD |
rs2472188 | chr2:113063237 | C>G | SNV | IL36RN : 3 Prime UTR Variant | ND |
rs2072134 | chr12:112971371 | G>A | SNV | OAS3 : 3 Prime UTR Variant | AD |
rs9876981 | chr3:112885405 | G>T | SNV | Intergenic | AD |
rs17042517 | chr2:112882007 | A>G | SNV | Intergenic | AD |
rs2708914 | chr2:112869657 | T>G | SNV | Intergenic | AD |
rs6746923 | chr2:112795849 | A>G | SNV | Intergenic | AD |
rs7806781 | chr7:112780017 | C>A / C>T | SNV | TMEM168 : Intron Variant | AD |
rs3790598 | chr1:112654274 | G>A / G>T | SNV | CAPZA1 : Intron Variant | AD |
rs9387092 | chr6:112643150 | C>T | SNV | Intergenic | AD |
rs77409651 | chr10:112642215 | T>A | SNV | VTI1A : Intron Variant | CD |
rs13146963 | chr4:112637446 | A>G | SNV | LARP7 : Intron Variant ZGRF1 : 2KB Upstream Variant | AD |
rs2087111 | chr4:112614924 | A>G / A>T | SNV | ZGRF1 : Intron Variant | AD |
rs9307383 | chr4:112608678 | C>T | SNV | ZGRF1 : Intron Variant | AD |
rs2029211 | chr4:112566978 | T>C | SNV | ZGRF1 : Intron Variant | AD |
rs9991830 | chr4:112564216 | T>C | SNV | ZGRF1 : Intron Variant | AD |
rs4833414 | chr4:112548757 | T>C | SNV | ZGRF1 : Intron Variant | AD |
rs1486865 | chr4:112544495 | A>G | SNV | ZGRF1 : Intron Variant LOC105377372 : Intron Variant | AD |
rs143894582 | chr12:112469070-112469078 | dupA | Indel | PTPN11 : Intron Variant | AD |
rs7919710 | chr10:112409794 | G>A | SNV | ACSL5 : Intron Variant | AD |
rs11066280 | chr12:112379979 | T>A | SNV | HECTD4 : Intron Variant | AD |
rs1420852 | chr8:112252548 | C>G | SNV | CSMD3 : Intron Variant | CD |
rs6995441 | chr8:112243993 | T>C | SNV | CSMD3 : Intron Variant | CD |
rs4876460 | chr8:112234021 | T>C | SNV | CSMD3 : Intron Variant | AD |
rs9307379 | chr4:112229132 | G>C / G>T | SNV | Intergenic | AD |
rs9549880 | chr13:112207874 | G>A / G>T | SNV | Intergenic | AD |
rs2074356 | chr12:112207597 | G>A | SNV | HECTD4 : Intron Variant | AD |
rs9324268 | chr13:112182341 | C>T | SNV | LOC105370370 : Non Coding Transcript Variant | AD |
rs11066173 | chr12:112116863 | A>G | SNV | Intergenic | AD |
rs3825388 | chr12:112048147 | G>A | SNV | NAA25 : Intron Variant | AD |
rs3814026 | chr2:111884089 | T>C | SNV | ANAPC1 : 5 Prime UTR Variant | ND |
rs9653414 | chr2:111877160 | G>A | SNV | ANAPC1 : Intron Variant | ND |
rs10197222 | chr2:111869646 | A>G | SNV | ANAPC1 : Intron Variant | ND |
rs6742515 | chr2:111867998 | T>C / T>G | SNV | ANAPC1 : Intron Variant | ND |
rs11066053 | chr12:111866549 | G>A | SNV | MAPKAPK5 : Intron Variant | AD |
rs736534 | chr12:111826996 | G>A | SNV | Intergenic | AD |
rs10849971 | chr12:111813393 | A>G | SNV | Intergenic | AD |
rs671 | chr12:111803962 | G>A | SNV | ALDH2 : Missense Variant | AD |
rs11066019 | chr12:111746083 | A>G | SNV | ACAD10 : Intron Variant | AD |
rs11066015 | chr12:111730205 | G>A | SNV | ACAD10 : Intron Variant | AD |
rs42283 | chr5:111704625 | G>A | SNV | STARD4-AS1 : Intron Variant | AD |
rs9308632 | chr2:111684984 | T>C | SNV | Intergenic | ND |
rs9308631 | chr2:111684854 | G>A | SNV | Intergenic | ND |
rs3782886 | chr12:111672685 | T>C | SNV | BRAP : Missense Variant | AD |
rs6754001 | chr2:111670832 | A>G | SNV | Intergenic | ND |
rs1399665 | chr2:111667963 | A>G | SNV | Intergenic | AD |
rs10849964 | chr12:111630634 | A>G | SNV | Intergenic | AD |
rs7969300 | chr12:111555908 | C>T | SNV | ATXN2 : Missense Variant | AD |
rs149212747 | chr12:111398968-111398974 | dupC | Indel | LOC105369984 : Intron Variant | AD |
rs4356268 | chr11:111379925 | A>G | SNV | POU2AF1 : 2KB Upstream Variant | AD |
rs2479956 | chr13:111329052 | T>C | SNV | TEX29 : Intron Variant | AD |
rs2479955 | chr13:111328131 | A>G | SNV | TEX29 : Intron Variant | AD |
rs4839122 | chr1:111311585 | T>C | SNV | CHIA : Intron Variant | AD |
rs4240530 | chr1:111310959 | C>T | SNV | CHIA : Intron Variant | AD |
rs6962665 | chr7:111309510 | C>A | SNV | IMMP2L : Intron Variant | AD |
rs3742179 | chr13:111305738 | T>C | SNV | TEX29 : 2KB Upstream Variant ARHGEF7 : 500B Downstream Variant | ND |
rs11534045 | chr7:111295923 | G>A | SNV | IMMP2L : Intron Variant | AD |
rs4766566 | chr12:111269073 | C>T | SNV | CUX2 : Intron Variant | AD |
rs6490029 | chr12:111260653 | G>A | SNV | CUX2 : Intron Variant | AD |
rs4766453 | chr12:111254320 | C>T | SNV | CUX2 : Intron Variant | AD |
rs1490901 | chr4:111236642 | G>A | SNV | Intergenic | AD |
rs7069564 | chr10:111137312 | C>T | SNV | Intergenic | CD |
rs945333 | chr10:111102271 | T>A / T>C | SNV | Intergenic | AD |
rs11593780 | chr10:111098817 | C>G / C>T | SNV | Intergenic | AD |
rs11781492 | chr8:111086064 | G>A | SNV | Intergenic | AD |
rs11195397 | chr10:110990871 | C>T | SNV | SHOC2 : Intron Variant | AD |
rs12229654 | chr12:110976657 | T>G | SNV | Intergenic | AD |
rs10774610 | chr12:110902439 | T>C | SNV | CCDC63 : Intron Variant | AD |
rs1858881 | chr12:110896313 | T>C | SNV | CCDC63 : Intron Variant | AD |
rs10849915 | chr12:110895818 | T>C | SNV | CCDC63 : Intron Variant | AD |
rs11065750 | chr12:110893212 | G>A | SNV | CCDC63 : Intron Variant | AD |
rs10488719 | chr11:110877346 | G>A | SNV | Intergenic | AD |
rs2238149 | chr12:110874125 | T>C | SNV | CCDC63 : Intron Variant | AD |
rs7513168 | chr1:110870290 | T>C | SNV | CD53 : 2KB Upstream Variant | AD |
rs6701134 | chr1:110864277 | A>G | SNV | Intergenic | AD |
rs6690536 | chr1:110854829 | T>C | SNV | Intergenic | AD |
rs6687898 | chr1:110854694 | A>G | SNV | Intergenic | AD |
rs6687919 | chr1:110854554 | T>G | SNV | Intergenic | AD |
rs6672672 | chr1:110854468 | C>T | SNV | Intergenic | AD |
rs12730405 | chr1:110854293 | A>G | SNV | Intergenic | AD |
rs718463 | chr1:110853984 | G>A | SNV | Intergenic | AD |
rs4631693 | chr1:110853466 | C>T | SNV | Intergenic | AD |
rs6685538 | chr1:110851000 | G>A | SNV | Intergenic | AD |
rs509276 | chr9:110819079 | G>A | SNV | Intergenic | AD |
rs343819 | chr1:110799868 | C>G / C>T | SNV | Intergenic | AD |
rs1462307 | chr3:110783001 | T>C | SNV | Intergenic | AD |
rs420033 | chr1:110753052 | G>A | SNV | LOC105378901 : Intron Variant | AD |
rs41453452 | chr1:110752428 | G>C | SNV | LOC105378901 : Non Coding Transcript Variant | AD |
rs7572507 | chr2:110733154 | C>T | SNV | ACOXL : Intron Variant | AD |
rs2640480 | chr1:110670626 | C>A | SNV | KCNA3 : Intron Variant LOC107985174 : Intron Variant | AD |
rs1319782 | chr1:110668911 | C>T | SNV | KCNA3 : Intron Variant LOC107985174 : Intron Variant | AD |
rs2640482 | chr1:110667697 | C>A | SNV | KCNA3 : Intron Variant LOC107985174 : Intron Variant | AD |
rs7082195 | chr10:110667691 | C>T | SNV | RBM20 : Intron Variant | ND |
rs2640487 | chr1:110664263 | C>T | SNV | KCNA3 : Intron Variant LOC107985174 : Intron Variant | AD |
rs2797533 | chr1:110644162 | C>G / C>T | SNV | LOC107985174 : Intron Variant | AD |
rs1856801 | chr10:110632404 | G>T | SNV | Intergenic | ND |
rs2724432 | chr11:110413469 | C>T | SNV | Intergenic | ND |
rs17358933 | chr1:110306583 | G>A | SNV | LOC440600 : Intron Variant | AD |
rs5942915 | chrX:110305798 | G>A | SNV | AMMECR1 : Intron Variant | AD |
rs6799277 | chr3:110255229 | C>T | SNV | Intergenic | AD |
rs9883805 | chr3:110242347 | A>G | SNV | Intergenic | AD |
rs17254838 | chrX:110228132 | T>G | SNV | AMMECR1 : Intron Variant | AD |
rs672949 | chr13:110227207 | C>T | SNV | COL4A1 : Intron Variant | ND |
rs10125067 | chr9:110171501 | A>G | SNV | AKAP2 : 3 Prime UTR Variant PALM2-AKAP2 : 3 Prime UTR Variant | AD |
rs514341 | chr1:110110258 | C>T | SNV | Intergenic | AD |
rs6930781 | chr6:110006481 | A>C / A>T | SNV | Intergenic | AD |
rs925368 | chr12:109953174 | T>C | SNV | GIT2 : Missense Variant | AD |
rs16940688 | chr12:109922516 | G>A | SNV | Intergenic | AD |
rs4245542 | chr6:109910795 | T>C | SNV | Intergenic | AD |
rs74416240 | chr12:109904793 | G>A | SNV | TCHP : Synonymous Variant | AD |
rs6492218 | chr13:109673402 | C>T | SNV | Intergenic | AD |
rs9996730 | chr4:109648939 | G>T | SNV | CCDC109B : Intron Variant | ND |
rs17161951 | chr5:109594889 | C>T | SNV | Intergenic | AD |
rs12640500 | chr4:109588030 | G>T | SNV | CCDC109B : Intron Variant | AD |
rs6537803 | chr1:109520918 | G>A | SNV | LOC105378893 : Intron Variant | AD |
rs6677291 | chr1:109513504 | C>T | SNV | Intergenic | AD |
rs7448843 | chr5:109508233 | A>C / A>T | SNV | LOC105379117 : Intron Variant | AD |
rs7092048 | chr10:109437972 | T>C | SNV | Intergenic | AD |
rs4134382 | chr13:109304942 | T>C | SNV | Intergenic | AD |
rs6857726 | chr4:109273128 | C>A / C>T | SNV | COL25A1 : Intron Variant | AD |
rs7322415 | chr13:109264613 | C>T | SNV | Intergenic | AD |
rs9515035 | chr13:109262482 | A>G | SNV | Intergenic | AD |
rs9515034 | chr13:109260209 | C>T | SNV | Intergenic | AD |
rs12684047 | chr9:109210391 | T>A | SNV | EPB41L4B : Intron Variant | ND |
rs2181666 | chr13:109204497 | A>G | SNV | MYO16 : Intron Variant | AD |
rs4365877 | chr5:109188915 | G>A | SNV | FER : 3 Prime UTR Variant | AD |
rs10759332 | chr9:109171981 | A>G | SNV | EPB41L4B : 3 Prime UTR Variant | ND |
rs919597 | chr13:109133497 | C>T | SNV | MYO16 : Intron Variant | AD |
rs1509718 | chr11:109120846 | C>T | SNV | Intergenic | AD |
rs17633258 | chr11:109115147 | C>G / C>T | SNV | Intergenic | ND |
rs17633211 | chr11:109114778 | T>C | SNV | Intergenic | ND |
rs17706334 | chr11:109110137 | A>G | SNV | Intergenic | ND |
rs17706299 | chr11:109110090 | C>G | SNV | Intergenic | ND |
rs2044590 | chr3:109007137 | G>A / G>C | SNV | MORC1 : Intron Variant | AD |
rs7933931 | chr11:108955180 | A>G | SNV | Intergenic | CD |
rs2715689 | chr3:108918583 | G>T | SNV | GUCA1C : Intron Variant | ND |
rs848353 | chr7:108908603 | A>G | SNV | Intergenic | ND |
rs1404697 | chr7:108904404 | G>C | SNV | Intergenic | ND |
rs564376 | chr6:108710797 | T>C | SNV | Intergenic | AD |
rs514293 | chr6:108703075 | C>T | SNV | Intergenic | AD |
rs11616603 | chr13:108519067 | A>G | SNV | MYO16 : Intron Variant | AD |
rs12146448 | chr11:108513934 | C>A / C>T | SNV | EXPH5 : Missense Variant LOC101928561 : Intron Variant | AD |
rs9587583 | chr13:108437268 | G>A | SNV | Intergenic | AD |
rs17040470 | chr12:108409978 | G>A | SNV | Intergenic | AD |
rs11113857 | chr12:108405096 | T>C | SNV | Intergenic | AD |
rs989001 | chr5:108340620 | G>A | SNV | FBXL17 : Intron Variant | ND |
rs1412427 | chr9:108178080 | C>T | SNV | LOC105376214 : Intron Variant | AD |
rs1412428 | chr9:108178039 | G>A | SNV | LOC105376214 : Intron Variant | AD |
rs4542003 | chr9:108160738 | T>C | SNV | LOC105376214 : Intron Variant | AD |
rs7794978 | chr7:108124785 | C>A / C>T | SNV | LAMB4 : Intron Variant | AD |
rs374810 | chr8:108083801 | G>A | SNV | RSPO2 : 2KB Upstream Variant | AD |
rs4956145 | chr4:108009883 | T>C | SNV | HADH : Missense Variant | ND |
rs12514413 | chr5:107988165 | T>C | SNV | FBXL17 : Intron Variant | ND |
rs10793832 | chr5:107984529 | T>A / T>C | SNV | FBXL17 : Intron Variant | ND |
rs11744308 | chr5:107974502 | A>T | SNV | FBXL17 : Intron Variant | ND |
rs885624 | chr5:107964954 | T>A / T>C | SNV | FBXL17 : Intron Variant | ND |
rs10979126 | chr9:107949884 | G>A | SNV | LOC105376211 : 2KB Upstream Variant | AD |
rs10069340 | chr5:107898090 | G>A | SNV | FBXL17 : Intron Variant | AD |
rs632582 | chr6:107853969 | G>A | SNV | Intergenic | AD |
rs6891749 | chr5:107803280 | G>A | SNV | Intergenic | AD |
rs770172 | chr5:107785718 | A>G | SNV | Intergenic | AD |
rs770182 | chr5:107782439 | G>T | SNV | Intergenic | AD |
rs328026 | chr2:107764075 | C>T | SNV | GACAT1 : Intron Variant | ND |
rs7787927 | chr7:107763915 | C>A | SNV | CBLL1 : 3 Prime UTR Variant | AD |
rs12705421 | chr7:107760984 | A>G | SNV | CBLL1 : Non Coding Transcript Variant | AD |
rs4730258 | chr7:107755787 | A>G | SNV | CBLL1 : Intron Variant | AD |
rs13226711 | chr7:107754897 | G>A | SNV | CBLL1 : Intron Variant | AD |
rs10280767 | chr7:107752975 | C>A | SNV | CBLL1 : Intron Variant | AD |
rs2188565 | chr7:107750624 | G>A | SNV | CBLL1 : Intron Variant | AD |
rs2023712 | chr7:107749842 | C>T | SNV | CBLL1 : Intron Variant | AD |
rs13231387 | chr7:107749534 | C>T | SNV | CBLL1 : Intron Variant | AD |
rs6956243 | chr7:107748466 | T>C | SNV | CBLL1 : Intron Variant | AD |
rs10808154 | chr7:107745951 | G>A | SNV | CBLL1 : Intron Variant LOC101927974 : 2KB Upstream Variant | AD |
rs7782475 | chr7:107745806 | C>T | SNV | CBLL1 : Intron Variant LOC101927974 : 2KB Upstream Variant | AD |
rs2188563 | chr7:107733426 | G>A | SNV | Intergenic | AD |
rs10953545 | chr7:107731890 | T>C | SNV | Intergenic | AD |
rs4727685 | chr7:107731613 | G>A | SNV | Intergenic | AD |
rs2157949 | chr7:107729091 | G>A | SNV | Intergenic | AD |
rs4730253 | chr7:107720991 | A>G | SNV | Intergenic | AD |
rs4730252 | chr7:107720852 | C>T | SNV | Intergenic | AD |
rs10265205 | chr7:107719678 | G>A | SNV | Intergenic | AD |
rs2712218 | chr7:107716314 | G>A | SNV | SLC26A4 : 3 Prime UTR Variant | AD |
rs2712207 | chr7:107711672 | G>A | SNV | SLC26A4 : Intron Variant | AD |
rs2712208 | chr7:107703317 | C>G | SNV | SLC26A4 : Intron Variant | AD |
rs982915 | chr7:107699466 | G>A | SNV | SLC26A4 : Intron Variant | AD |
rs2188561 | chr7:107695613 | C>A / C>T | SNV | SLC26A4 : Intron Variant | AD |
rs2237679 | chr7:107693581 | C>T | SNV | SLC26A4 : Intron Variant | AD |
rs1858930 | chr7:107688092 | A>C | SNV | SLC26A4 : Intron Variant | AD |
rs2712210 | chr7:107687407 | C>T | SNV | SLC26A4 : Intron Variant | AD |
rs10890750 | chr11:107678793 | G>A | SNV | Intergenic | AD |
rs6881619 | chr5:107573359 | T>C | SNV | EFNA5 : Intron Variant | ND |
rs7775895 | chr6:107565318 | G>A / G>T | SNV | SOBP : Intron Variant | AD |
rs1913586 | chr4:107534064 | T>A / T>C | SNV | Intergenic | AD |
rs17037826 | chr4:107528681 | A>C | SNV | Intergenic | AD |
rs10511260 | chr3:107514250 | T>G | SNV | Intergenic | AD |
rs10511261 | chr3:107483777 | C>A | SNV | Intergenic | AD |
rs1429 | chr3:107468497 | C>T | SNV | Intergenic | AD |
rs1850344 | chr3:107466226 | A>G | SNV | Intergenic | AD |
rs1323806 | chr9:107243804 | C>T | SNV | Intergenic | AD |
rs17037483 | chr4:107178564 | A>C | SNV | Intergenic | AD |
rs17037473 | chr4:107173493 | G>A | SNV | Intergenic | AD |
rs7694364 | chr4:107163457 | T>C | SNV | Intergenic | AD |
rs2769920 | chr13:107141642 | A>G | SNV | Intergenic | ND |
rs11193198 | chr10:107102209 | G>A | SNV | SORCS1 : Intron Variant | AD |
rs17787921 | chr9:106869544 | C>T | SNV | ZNF462 : Intron Variant | AD |
rs10890597 | chr11:106804584 | A>G | SNV | GUCY1A2 : Intron Variant | AD |
rs7753899 | chr6:106744206 | C>T | SNV | LOC107986628 : Non Coding Transcript Variant LOC100422737 : Intron Variant | AD |
rs9480703 | chr6:106742549 | A>C | SNV | LOC100422737 : Intron Variant | AD |
rs9587180 | chr13:106708053 | A>G | SNV | Intergenic | AD |
rs6996005 | chr8:106520699 | T>G | SNV | OXR1 : Intron Variant LOC105375700 : Intron Variant | AD |
rs10933849 | chr3:106420954 | C>T | SNV | LOC101929485 : Intron Variant | AD |
rs618453 | chr11:106362367 | A>G / A>T | SNV | Intergenic | ND |
rs563816 | chr11:106360417 | C>T | SNV | Intergenic | ND |
rs9587100 | chr13:106179438 | A>G | SNV | Intergenic | AD |
rs6466086 | chr7:106122980 | A>G | SNV | Intergenic | AD |
rs10206195 | chr2:106097582 | T>C | SNV | UXS1 : Intron Variant | AD |
rs6923608 | chr6:106089915 | G>A / G>C | SNV | PRDM1 : Intron Variant | ND |
rs1404170 | chr5:106069466 | T>C | SNV | Intergenic | AD |
rs17332369 | chrX:106034774 | T>A | SNV | SERPINA7 : Intron Variant | AD |
rs4483718 | chr13:105998395 | T>A / T>G | SNV | Intergenic | ND |
rs609665 | chr11:105973338 | C>T | SNV | GRIA4 : Intron Variant | AD |
rs17152264 | chr7:105907952 | A>G | SNV | CDHR3 : Intron Variant | ND |
rs9519839 | chr13:105904212 | G>A | SNV | Intergenic | CD |
rs1482912 | chr5:105781902 | C>T | SNV | Intergenic | AD |
rs4590982 | chr12:105711045 | G>A | SNV | CASC18 : Intron Variant | ND |
rs9372096 | chr6:105617855 | C>T | SNV | LOC105377922 : Intron Variant | AD |
rs1706923 | chr7:105580650 | A>G | SNV | EFCAB10 : Intron Variant | AD |
rs1037306 | chr8:105549049 | T>C | SNV | ZFPM2 : Intron Variant LOC105375696 : Intron Variant | ND |
rs2052383 | chr13:105547179 | G>A / G>T | SNV | Intergenic | ND |
rs302964 | chr8:105506184 | C>T | SNV | ZFPM2 : Intron Variant | ND |
rs302960 | chr8:105505449 | A>G | SNV | ZFPM2 : Intron Variant | ND |
rs2149592 | chr9:105467709 | A>G | SNV | FSD1L : Intron Variant | ND |
rs2082371 | chr12:105440189 | A>G | SNV | LOC105369955 : Intron Variant LOC105369956 : Intron Variant | AD |
rs10746034 | chr12:105433635 | C>T | SNV | LOC105369955 : Intron Variant LOC105369956 : Intron Variant | AD |
rs2880439 | chr8:105256967 | A>G | SNV | Intergenic | AD |
rs11605652 | chr11:105197312 | G>A | SNV | Intergenic | AD |
rs10861359 | chr12:105168213 | C>A | SNV | KIAA1033 : Non Coding Transcript Variant | AD |
rs10133292 | chr14:104990824 | T>C | SNV | C14orf79 : Intron Variant | AD |
rs10083490 | chr14:104936081 | C>T | SNV | PLD4 : Intron Variant | AD |
rs2841269 | chr14:104919812 | G>C | SNV | Intergenic | AD |
rs2891786 | chr7:104918492 | C>T | SNV | LHFPL3-AS2 : Intron Variant | AD |
rs11761950 | chr7:104675698 | G>A | SNV | LHFPL3 : Intron Variant | ND |
rs10254402 | chr7:104551951 | T>C / T>G | SNV | LHFPL3 : Intron Variant | ND |
rs1704904 | chr12:104548608 | C>T | SNV | CHST11 : Intron Variant | ND |
rs17029932 | chr2:104542318 | G>A | SNV | Intergenic | AD |
rs11112082 | chr12:104497619 | G>T | SNV | CHST11 : Intron Variant | ND |
rs115357105 | chr9:104376689 | A>G | SNV | Intergenic | AD |
rs10861184 | chr12:104270315 | A>G | SNV | TXNRD1 : Intron Variant | AD |
rs1868009 | chr8:104256541 | G>T | SNV | Intergenic | ND |
rs6949887 | chr7:104196893 | G>A | SNV | ORC5 : Intron Variant | AD |
rs10260238 | chr7:104196532 | C>T | SNV | ORC5 : Intron Variant | AD |
rs2385134 | chr7:104169681 | G>A | SNV | ORC5 : Intron Variant | AD |
rs6765661 | chr3:103929476 | A>G | SNV | Intergenic | AD |
rs4132806 | chr3:103916591 | C>T | SNV | Intergenic | AD |
rs12573437 | chr10:103843405 | C>A | SNV | SH3PXD2A : Intron Variant | AD |
rs4145648 | chr5:103840533 | T>C | SNV | LOC105379107 : Intron Variant | AD |
rs2283029 | chr7:103757772 | T>C | SNV | RELN : Intron Variant | ND |
rs4370037 | chr3:103703268 | G>A | SNV | Intergenic | AD |
rs16846607 | chr3:103685267 | T>C | SNV | Intergenic | AD |
rs2403199 | chr14:103595731 | A>C | SNV | Intergenic | AD |
rs1396554 | chr9:103583028 | A>G | SNV | Intergenic | AD |
rs7452689 | chr6:103569094 | G>A / G>T | SNV | LOC105377916 : Intron Variant | AD |
rs75686122 | chr8:103561561 | C>A / C>T | SNV | RIMS2 : Intron Variant | CD |
rs9299372 | chr9:103541971 | A>C | SNV | Intergenic | AD |
rs7768059 | chr6:103327431 | G>T | SNV | Intergenic | AD |
rs4907992 | chr1:103297696 | A>G | SNV | Intergenic | AD |
rs17374436 | chr11:103185951 | T>C | SNV | DYNC2H1 : Intron Variant | AD |
rs9832587 | chr3:103115956 | T>A / T>C | SNV | Intergenic | AD |
rs11691730 | chr2:102944668 | G>A | SNV | Intergenic | ND |
rs6998032 | chr8:102931186 | C>T | SNV | AZIN1-AS1 : Intron Variant | AD |
rs1241182 | chr1:102882544 | A>C | SNV | COL11A1 : Intron Variant | AD |
rs12052617 | chr2:102862176 | G>A | SNV | Intergenic | ND |
rs2304348 | chr8:102833298 | A>C | SNV | AZIN1 : Intron Variant LOC107986873 : Intron Variant | AD |
rs9860789 | chr3:102748207 | A>G | SNV | Intergenic | AD |
rs9873502 | chr3:102717678 | G>T | SNV | LOC105374017 : Intron Variant | AD |
rs2513929 | chr8:102702118 | C>T | SNV | LOC101927245 : Intron Variant | AD |
rs10212345 | chr3:102688134 | C>T | SNV | LOC105374016 : Non Coding Transcript Variant | AD |
rs6726894 | chr2:102680477 | C>A / C>G | SNV | SLC9A2 : Intron Variant | AD |
rs7110424 | chr11:102552935 | G>T | SNV | Intergenic | AD |
rs10778176 | chr12:102469201 | C>A / C>T | SNV | IGF1 : Intron Variant | AD |
rs5742629 | chr12:102463485 | T>C | SNV | IGF1 : Intron Variant LOC105369942 : Non Coding Transcript Variant | AD |
rs11927186 | chr3:102192214 | C>A | SNV | Intergenic | ND |
rs7322577 | chr13:102184424 | T>A / T>G | SNV | FGF14 : Intron Variant | AD |
rs2619283 | chr3:102172051 | G>A | SNV | Intergenic | ND |
rs1190596 | chr14:102129288 | A>G | SNV | HSP90AA1 : Intron Variant | AD |
rs2155235 | chr8:102055399 | C>T | SNV | NCALD : Intron Variant | ND |
rs7324177 | chr13:101975249 | G>A | SNV | FGF14 : Intron Variant | AD |
rs12731963 | chr1:101916848 | T>C | SNV | OLFM3 : Intron Variant | ND |
rs1612684 | chr14:101909875 | G>T | SNV | PPP2R5C : Intron Variant | ND |
rs1336798 | chr1:101886314 | T>C | SNV | OLFM3 : Intron Variant DNAJA1P5 : Intron Variant | ND |
rs4907956 | chr1:101847147 | G>T | SNV | OLFM3 : Intron Variant | AD | ND |
rs12544026 | chr8:101819970 | G>A | SNV | NCALD : Intron Variant | AD |
rs1938831 | chr11:101665605 | T>C | SNV | Intergenic | AD |
rs9554813 | chr13:101639227 | A>G | SNV | ITGBL1 : Intron Variant | AD |
rs16867971 | chr8:101597228 | T>C | SNV | GRHL2 : Intron Variant | AD |
rs7299475 | chr12:101550400 | A>G | SNV | Intergenic | AD |
rs9518426 | chr13:101509729 | C>T | SNV | ITGBL1 : Intron Variant | AD |
rs6570989 | chr6:101509537 | G>A | SNV | GRIK2 : Intron Variant | ND |
rs4727494 | chr7:101438517 | G>A | SNV | COL26A1 : Intron Variant | ND |
rs17760784 | chr10:101396659 | G>C | SNV | BTRC : Intron Variant | ND |
rs7313312 | chr12:101361905 | T>A / T>C | SNV | UTP20 : Intron Variant | AD |
rs11609516 | chr12:101361142 | C>G | SNV | UTP20 : Intron Variant | AD |
rs10507130 | chr12:101360176 | G>A | SNV | UTP20 : Intron Variant | AD |
rs57083693 | chr12:101348402 | T>C | SNV | UTP20 : Intron Variant | AD |
rs3782848 | chr12:101346082 | G>A | SNV | UTP20 : Intron Variant | AD |
rs2270861 | chr12:101342603 | A>G | SNV | UTP20 : Intron Variant | AD |
rs7977587 | chr12:101340906 | A>G | SNV | UTP20 : Intron Variant | AD |
rs56265469 | chr12:101338877 | C>T | SNV | UTP20 : Synonymous Variant | AD |
rs1814577 | chr12:101335504 | A>G | SNV | UTP20 : Intron Variant | AD |
rs7973083 | chr12:101330303 | T>A | SNV | UTP20 : Intron Variant | AD |
rs55721648 | chr12:101321424 | C>A / C>T | SNV | UTP20 : Intron Variant | AD |
rs9433784 | chr1:101318784 | G>T | SNV | Intergenic | AD |
rs1472556 | chr12:101311400 | C>A | SNV | UTP20 : Intron Variant | AD |
rs7296572 | chr12:101296439 | C>T | SNV | UTP20 : Intron Variant | AD |
rs11608415 | chr12:101294267 | C>T | SNV | UTP20 : Intron Variant | AD |
rs844030 | chr12:101291644 | G>A | SNV | UTP20 : Intron Variant | AD |
rs703711 | chr12:101280507 | G>C | SNV | UTP20 : Intron Variant | AD |
rs824310 | chr12:101276878 | T>A | SNV | Intergenic | AD |
rs2651251 | chr12:101275238 | C>T | SNV | Intergenic | AD |
rs703720 | chr12:101274049 | G>T | SNV | Intergenic | AD |
rs703717 | chr12:101272239 | A>G | SNV | Intergenic | AD |
rs7532171 | chr1:101259395 | C>T | SNV | Intergenic | ND |
rs17417367 | chr1:101155173 | A>G | SNV | LOC101928334 : Intron Variant | AD |
rs7608232 | chr2:101082601 | C>A | SNV | TBC1D8 : Intron Variant | AD |
rs701837 | chr10:101015448 | T>C | SNV | PDZD7 : Intron Variant | AD |
rs2054128 | chr15:101001562 | G>A | SNV | LRRK1 : Intron Variant | ND |
rs8038607 | chr15:100974424 | T>C | SNV | LRRK1 : Intron Variant | ND |
rs12911894 | chr15:100953634 | C>A | SNV | LRRK1 : Intron Variant | AD |
rs7911957 | chr10:100933213 | A>G | SNV | SLF2 : Intron Variant | AD |
rs12241232 | chr10:100932847 | T>C | SNV | SLF2 : Intron Variant | AD |
rs4917916 | chr10:100913535 | G>A | SNV | SLF2 : Intron Variant | AD |
rs3802724 | chr10:100912961 | T>C | SNV | SLF2 : Non Coding Transcript Variant | AD |
rs3809404 | chr14:100889673 | A>C / A>G | SNV | Intergenic | AD |
rs12632235 | chr3:100817440 | C>T | SNV | ABI3BP : Synonymous Variant | AD |
rs13250895 | chr8:100802097 | G>C | SNV | Intergenic | AD |
rs13249189 | chr8:100801674 | C>T | SNV | Intergenic | AD |
rs13279103 | chr8:100801569 | T>A / T>C | SNV | Intergenic | AD |
rs10955242 | chr8:100801402 | G>A | SNV | Intergenic | AD |
rs3843552 | chr8:100801040 | G>A / G>T | SNV | Intergenic | AD |
rs3847154 | chr8:100800950 | C>T | SNV | Intergenic | AD |
rs3847153 | chr8:100800928 | A>G | SNV | Intergenic | AD |
rs3847152 | chr8:100800846 | C>A / C>T | SNV | Intergenic | AD |
rs3843551 | chr8:100800817 | A>G | SNV | Intergenic | AD |
rs13276772 | chr8:100800709 | T>C | SNV | Intergenic | AD |
rs13274060 | chr8:100800599 | A>T | SNV | Intergenic | AD |
rs7013576 | chr8:100800172 | T>C | SNV | Intergenic | AD |
rs7012929 | chr8:100799769 | T>G | SNV | Intergenic | AD |
rs7016480 | chr8:100799162 | C>T | SNV | Intergenic | AD |
rs7016174 | chr8:100799020 | A>C | SNV | Intergenic | AD |
rs7016436 | chr8:100798996 | G>A | SNV | Intergenic | AD |
rs7016087 | chr8:100798708 | G>A | SNV | Intergenic | AD |
rs10808368 | chr8:100798618 | T>G | SNV | Intergenic | AD |
rs6993814 | chr8:100798504 | T>G | SNV | Intergenic | AD |
rs10808367 | chr8:100798423 | C>G | SNV | Intergenic | AD |
rs10808366 | chr8:100798419 | T>G | SNV | Intergenic | AD |
rs10808365 | chr8:100798263 | T>C | SNV | Intergenic | AD |
rs3847151 | chr8:100797572 | A>G | SNV | Intergenic | AD |
rs59317432 | chr8:100797434 | G>A | SNV | Intergenic | AD |
rs60243676 | chr8:100797285 | C>G | SNV | Intergenic | AD |
rs58751921 | chr8:100796737 | A>G | SNV | Intergenic | AD |
rs10464815 | chr8:100795923 | A>C | SNV | Intergenic | AD |
rs35866478 | chr8:100795137 | G>A | SNV | Intergenic | AD |
rs36061340 | chr8:100795002 | C>T | SNV | Intergenic | AD |
rs61101261 | chr8:100793827 | C>A | SNV | Intergenic | AD |
rs11097740 | chr4:100793800 | C>T | SNV | Intergenic | AD |
rs4703116 | chr5:100793209 | T>C | SNV | Intergenic | AD |
rs278496 | chr5:100764453 | T>C | SNV | Intergenic | AD |
rs3176874 | chr1:100734330 | A>G | SNV | VCAM1 : Intron Variant | AD |
rs1765738 | chr13:100730836 | C>G | SNV | NALCN-AS1 : Intron Variant | AD |
rs8022367 | chr14:100723120 | A>T | SNV | Intergenic | AD |
rs17577580 | chr14:100722868 | C>T | SNV | Intergenic | AD |
rs9554711 | chr13:100624630 | A>G | SNV | TMTC4 : Intron Variant | ND |
rs10115383 | chr9:100608250 | A>G | SNV | Intergenic | ND |
rs4965678 | chr15:100575243 | C>A | SNV | LINS1 : Intron Variant | AD |
rs1493652 | chr15:100572137 | T>C | SNV | LINS1 : Non Coding Transcript Variant | AD |
rs3764198 | chr15:100570360 | C>A / C>T | SNV | LINS1 : Splice Donor Variant | AD |
rs11634945 | chr15:100553925 | C>T | SNV | PRKXP1 : Non Coding Transcript Variant | AD |
rs4928112 | chr3:100544715 | G>A | SNV | TMEM45A : Intron Variant | AD |
rs9390276 | chr6:100331816 | T>C | SNV | Intergenic | AD |
rs117557854 | chr11:100268439 | G>A | SNV | CNTN5 : Intron Variant | AD |
rs681561 | chr13:100246275 | A>C | SNV | PCCA : Intron Variant | AD |
rs5921523 | chrX:100224970 | A>C | SNV | Intergenic | AD |
rs2766692 | chr14:100217855 | A>G | SNV | Intergenic | AD |
rs1038235 | chr15:100195762 | T>C | SNV | ADAMTS17 : Intron Variant | ND |
rs79246196 | chr7:100185286 | C>T | SNV | STAG3 : Intron Variant | AD |
rs2573680 | chr15:100018820 | T>C | SNV | ADAMTS17 : Intron Variant | ND |
rs17112202 | chr10:99735234 | T>C | SNV | CUTC : Intron Variant | AD |
rs11813439 | chr10:99692612 | G>A | SNV | ENTPD7 : Intron Variant | AD |
rs4851222 | chr2:99672469 | G>A | SNV | AFF3 : Intron Variant | AD |
rs11676683 | chr2:99659463 | A>C | SNV | AFF3 : Intron Variant | AD |
rs2700648 | chr3:99388839 | G>A | SNV | Intergenic | AD |
rs1372680 | chr4:99383388 | C>A | SNV | LOC102723576 : Non Coding Transcript Variant | AD |
rs1826907 | chr4:99379969 | A>C | SNV | LOC102723576 : Intron Variant | AD |
rs2200019 | chr3:99377052 | C>T | SNV | Intergenic | AD |
rs2700586 | chr3:99375946 | C>T | SNV | Intergenic | AD |
rs10735366 | chr12:99372428 | G>A | SNV | ANKS1B : Intron Variant | ND |
rs72681920 | chr4:99369122 | C>A | SNV | Intergenic | AD |
rs2700667 | chr3:99366962 | G>A / G>C | SNV | Intergenic | AD |
rs4699741 | chr4:99357540 | T>C | SNV | Intergenic | AD |
rs1789924 | chr4:99353129 | C>T | SNV | ADH1C : 2KB Upstream Variant | AD |
rs34761493 | chr4:99352013 | G>A | SNV | ADH1C : Intron Variant | AD |
rs12639833 | chr4:99346215 | C>T | SNV | ADH1C : Intron Variant | AD |
rs1662051 | chr4:99346082 | C>A | SNV | ADH1C : Intron Variant | AD |
rs6532815 | chr4:99345999 | A>G | SNV | ADH1C : Intron Variant | AD |
rs2241894 | chr4:99344976 | T>A / T>C | SNV | ADH1C : Synonymous Variant | AD |
rs1789911 | chr4:99342621 | T>C | SNV | ADH1C : Intron Variant | AD |
rs904095 | chr4:99342226 | A>G | SNV | ADH1C : Intron Variant | AD |
rs1614972 | chr4:99336998 | C>T | SNV | ADH1C : Intron Variant | AD |
rs2298753 | chr4:99336750 | T>C | SNV | ADH1C : Non Coding Transcript Variant | AD |
rs1789896 | chr4:99335827 | G>A / G>T | SNV | Intergenic | AD |
rs1229978 | chr4:99335042 | T>C | SNV | Intergenic | AD |
rs2173201 | chr4:99329813 | C>A | SNV | Intergenic | AD |
rs1789891 | chr4:99329262 | C>A | SNV | Intergenic | AD |
rs9307239 | chr4:99325780 | C>T | SNV | Intergenic | AD |
rs1229984 | chr4:99318162 | T>C | SNV | ADH1B : Missense Variant | AD |
rs1693457 | chr4:99315605 | C>T | SNV | ADH1B : Intron Variant | AD |
rs1789882 | chr4:99313896 | A>G | SNV | ADH1B : Synonymous Variant | AD |
rs2066702 | chr4:99307860 | G>A | SNV | ADH1B : Missense Variant | AD |
rs904092 | chr4:99293007 | A>G / A>T | SNV | ADH1A : 2KB Upstream Variant LOC100507053 : Intron Variant | AD |
rs11109794 | chr12:99283218 | G>A | SNV | ANKS1B : Intron Variant | AD |
rs7035064 | chr9:99169458 | A>G | SNV | Intergenic | ND |
rs17028615 | chr4:99150767 | A>G | SNV | LOC100507053 : Intron Variant | AD |
rs4148883 | chr4:99145181 | T>C | SNV | ADH4 : 2KB Upstream Variant LOC100507053 : Intron Variant | AD |
rs6831352 | chr4:99142374 | T>A / T>C | SNV | ADH4 : Intron Variant LOC100507053 : Intron Variant | AD |
rs6532800 | chr4:99137733 | T>C / T>G | SNV | ADH4 : Intron Variant LOC100507053 : Intron Variant | AD |
rs6532798 | chr4:99133676 | C>T | SNV | ADH4 : Intron Variant LOC100507053 : Non Coding Transcript Variant | AD |
rs6822348 | chr4:99132743 | A>T | SNV | ADH4 : Intron Variant LOC100507053 : Intron Variant | AD |
rs1126670 | chr4:99131582 | C>A | SNV | ADH4 : Synonymous Variant LOC100507053 : Intron Variant | AD |
rs4699710 | chr4:99130668 | C>T | SNV | ADH4 : Intron Variant LOC100507053 : Intron Variant | AD |
rs6836440 | chr4:99127355 | G>A | SNV | ADH4 : Intron Variant LOC100507053 : Intron Variant | AD |
rs1126671 | chr4:99127263 | T>C | SNV | ADH4 : Missense Variant LOC100507053 : Intron Variant | AD |
rs17367186 | chr12:99126816 | T>G | SNV | ANKS1B : Intron Variant | AD |
rs1573495 | chr4:99125534 | T>C | SNV | ADH4 : Intron Variant LOC100507053 : Intron Variant | AD |
rs2372644 | chr12:99096982 | T>G | SNV | ANKS1B : Intron Variant LOC101928937 : Intron Variant | AD |
rs7031588 | chr9:99060020 | C>T | SNV | COL15A1 : Intron Variant | ND |
rs2487891 | chr10:99040075 | T>C | SNV | HPSE2 : Intron Variant | ND |
rs17166455 | chr5:98940235 | T>C | SNV | LOC102724810 : Intron Variant | ND |
rs10900866 | chr5:98751615 | T>C | SNV | Intergenic | AD |
rs4966017 | chr15:98724404 | T>A / T>C / T>G | SNV | IGF1R : Intron Variant | AD |
rs3803476 | chr15:98713341 | A>G | SNV | IGF1R : Intron Variant | AD |
rs4905720 | chr14:98587627 | A>G | SNV | Intergenic | AD |
rs8005917 | chr14:98586716 | T>C | SNV | Intergenic | AD |
rs705326 | chr7:98562879 | T>A / T>C / T>G | SNV | Intergenic | AD |
rs4641724 | chr15:98541531 | C>A | SNV | Intergenic | AD |
rs1461155 | chr3:98529888 | T>C | SNV | Intergenic | AD |
rs12719740 | chr15:98529676 | G>A | SNV | Intergenic | AD |
rs2779582 | chr9:98524835 | C>T | SNV | GABBR2 : Intron Variant | AD |
rs2779581 | chr9:98524703 | T>C | SNV | GABBR2 : Intron Variant | AD |
rs2779576 | chr9:98522270 | A>T | SNV | GABBR2 : Intron Variant | AD |
rs944760 | chr9:98521459 | G>T | SNV | GABBR2 : Intron Variant | AD |
rs2779569 | chr9:98518102 | T>C | SNV | GABBR2 : Intron Variant | AD |
rs2779556 | chr9:98503008 | A>C | SNV | GABBR2 : Intron Variant | AD |
rs2808560 | chr9:98499936 | C>T | SNV | GABBR2 : Intron Variant | AD |
rs874278 | chr9:98487141 | G>A | SNV | GABBR2 : Intron Variant | AD |
rs7161221 | chr14:98426546 | A>C | SNV | Intergenic | AD |
rs10141191 | chr14:98421173 | G>A | SNV | Intergenic | AD |
rs17310732 | chr8:98403209 | G>A / G>T | SNV | Intergenic | AD |
rs1459124 | chr14:98386551 | C>T | SNV | Intergenic | AD |
rs2772354 | chr13:98383634 | A>G | SNV | FARP1 : Intron Variant | AD |
rs873196 | chr14:98379194 | C>T | SNV | Intergenic | AD |
rs6984462 | chr8:98374366 | C>T | SNV | Intergenic | AD |
rs10865016 | chr2:98372841 | G>A / G>T | SNV | CNGA3 : Intron Variant | ND |
rs7075856 | chr10:98329453 | C>A | SNV | Intergenic | AD |
rs6870671 | chr5:98303039 | T>C | SNV | Intergenic | AD |
rs1414298 | chrX:98279846 | T>C | SNV | Intergenic | AD |
rs8025476 | chr15:98271069 | T>A / T>G | SNV | Intergenic | AD |
rs10115971 | chr9:98262605 | A>G | SNV | Intergenic | AD |
rs4608580 | chr2:98244594 | C>T | SNV | VWA3B : Intron Variant | ND |
rs16914086 | chr9:98226195 | G>A | SNV | TBC1D2 : Intron Variant | ND |
rs4735529 | chr8:98127382 | C>T | SNV | POP1 : Intron Variant | AD |
rs10808358 | chr8:98124925 | G>A | SNV | POP1 : Intron Variant | AD |
rs4734384 | chr8:98121450 | A>C | SNV | POP1 : Intron Variant | AD |
rs2071597 | chr8:98117421 | A>G | SNV | POP1 : Intron Variant RIDA : 2KB Upstream Variant | AD |
rs12148124 | chr15:98065464 | T>C | SNV | Intergenic | ND |
rs1391665 | chr3:97914893 | T>C | SNV | CRYBG3 : Intron Variant | AD |
rs4857068 | chr3:97903853 | C>A | SNV | CRYBG3 : Intron Variant | AD |
rs6496267 | chr15:97902567 | G>A | SNV | Intergenic | AD |
rs1498652 | chr3:97901684 | A>C | SNV | CRYBG3 : Intron Variant | AD |
rs6786354 | chr3:97876535 | G>A | SNV | CRYBG3 : Missense Variant | AD |
rs3856567 | chr3:97864832 | A>G | SNV | CRYBG3 : Intron Variant LOC105373994 : Intron Variant | AD |
rs699300 | chr3:97847729 | G>A | SNV | CRYBG3 : Intron Variant LOC105373994 : Intron Variant | AD |
rs1848035 | chr3:97823011 | C>T | SNV | CRYBG3 : Intron Variant LOC101929298 : 2KB Upstream Variant | AD |
rs6439361 | chr3:97753712 | G>A | SNV | EPHA6 : Non Coding Transcript Variant | AD |
rs7913179 | chr10:97705109 | C>A / C>G | SNV | Intergenic | AD |
rs2045966 | chr8:97581926 | C>G | SNV | Intergenic | ND |
rs184729 | chr13:97540481 | A>C / A>T | SNV | LOC105370324 : Intron Variant LOC105370325 : 2KB Upstream Variant | AD |
rs6795420 | chr3:97496739 | A>G | SNV | EPHA6 : Intron Variant | AD |
rs1379842 | chr3:97482906 | C>A / C>T | SNV | EPHA6 : Intron Variant | AD |
rs1598915 | chr3:97386708 | C>T | SNV | EPHA6 : Intron Variant LOC101929278 : Intron Variant | AD |
rs9556711 | chr13:97364162 | G>A | SNV | MBNL2 : Intron Variant | AD |
rs1556086 | chr13:97326231 | A>G | SNV | MBNL2 : Intron Variant | AD |
rs10980992 | chr9:97183759 | C>T | SNV | ANKRD18CP : Intron Variant | AD |
rs2282424 | chr13:97136192 | G>A / G>C | SNV | Intergenic | ND |
rs2535483 | chr15:97013682 | C>T | SNV | Intergenic | AD |
rs11188984 | chr10:97006464 | C>T | SNV | SLIT1 : Intron Variant | AD |
rs7124287 | chr11:96999233 | G>A / G>T | SNV | Intergenic | ND |
rs1207688 | chr7:96932719 | C>T | SNV | Intergenic | AD |
rs249571 | chr12:96927433 | C>T | SNV | NEDD1 : Intron Variant | AD |
rs17168021 | chr7:96913670 | T>C | SNV | Intergenic | AD |
rs9374164 | chr6:96866469 | T>C | SNV | Intergenic | AD |
rs13160562 | chr5:96775667 | G>A | SNV | ERAP1 : Intron Variant LOC102724748 : 2KB Upstream Variant | AD |
rs13362120 | chr5:96735490 | T>C | SNV | CAST : Intron Variant | AD |
rs11847777 | chr14:96687006 | G>C | SNV | Intergenic | ND |
rs12675345 | chr8:96673363 | C>A | SNV | CPQ : Intron Variant | AD |
rs7149784 | chr14:96591661 | G>A | SNV | Intergenic | AD |
rs4132568 | chr7:96505669 | A>C | SNV | LOC105375411 : Intron Variant | ND |
rs34717128 | chr11:96500639 | T>A | SNV | JRKL-AS1 : Intron Variant | CD |
rs7181753 | chr15:96301498 | C>T | SNV | NR2F2-AS1 : Intron Variant | AD |
rs2263190 | chr6:96291517 | T>C | SNV | Intergenic | AD |
rs4509239 | chr7:96264902 | C>A / C>T | SNV | SLC25A13 : Intron Variant | ND |
rs7322488 | chr13:96264380 | T>C | SNV | HS6ST3 : Intron Variant | ND |
rs4984530 | chr15:96263187 | T>C | SNV | NR2F2-AS1 : Intron Variant | AD |
rs4905470 | chr14:96226874 | G>A | SNV | BDKRB2 : Intron Variant | AD |
rs12417347 | chr11:96224040 | A>G | SNV | MAML2 : Intron Variant | AD |
rs4132260 | chr6:96147144 | C>T | SNV | FUT9 : Intron Variant | AD |
rs111325002 | chr3:96134788 | A>G | SNV | Intergenic | CD |
rs1036517 | chr15:96102971 | G>A | SNV | LOC105369212 : Intron Variant | AD |
rs7171368 | chr15:96094214 | T>C | SNV | LOC105369212 : Intron Variant | AD |
rs11636705 | chr15:96062683 | C>A / C>T | SNV | Intergenic | ND |
rs9788546 | chr14:96059129 | T>G | SNV | C14orf132 : Intron Variant | AD |
rs11847860 | chr14:96045680 | T>A / T>G | SNV | C14orf132 : Intron Variant | AD |
rs12890394 | chr14:96045020 | C>T | SNV | C14orf132 : Intron Variant | AD |
rs607395 | chr11:96023248 | G>A | SNV | MAML2 : Intron Variant | AD |
rs2039617 | chr10:95999446 | G>A | SNV | CC2D2B : Intron Variant ENTPD1-AS1 : Intron Variant | AD |
rs10759883 | chr9:95790481 | C>T | SNV | Intergenic | ND |
rs3949478 | chr10:95713457 | A>G | SNV | ENTPD1 : Intron Variant | ND |
rs854104 | chr7:95696422 | A>C / A>G | SNV | LOC105375409 : Intron Variant | AD |
rs854061 | chr7:95676056 | G>A / G>C | SNV | LOC105375409 : Intron Variant | AD |
rs1932075 | chr9:95597834 | C>T | SNV | Intergenic | AD |
rs7113885 | chr11:95562213 | A>C / A>T | SNV | Intergenic | ND |
rs16922195 | chr11:95559293 | A>G | SNV | Intergenic | ND |
rs11606101 | chr11:95557357 | T>C | SNV | Intergenic | ND |
rs2380220 | chr6:95519536 | T>C | SNV | Intergenic | AD |
rs933769 | chr15:95509513 | C>T | SNV | Intergenic | AD |
rs3857231 | chr4:95445291 | T>C | SNV | UNC5C : Intron Variant | AD |
rs569612 | chr11:95380889 | C>A | SNV | Intergenic | AD |
rs999986 | chr14:95337519 | C>A | SNV | Intergenic | ND |
rs7912686 | chr10:95266701 | T>C | SNV | PDLIM1 : Intron Variant | AD |
rs4148478 | chr13:95197426 | A>G | SNV | ABCC4 : Intron Variant | AD |
rs646667 | chr11:95182814 | T>C | SNV | SESN3 : Intron Variant | AD |
rs654499 | chr11:95110343 | C>A / C>T | SNV | ENDOD1 : Intron Variant | ND |
rs16950632 | chr13:95109632 | G>A | SNV | ABCC4 : Intron Variant | AD |
rs73459955 | chr15:95109294 | C>T | SNV | LOC105370991 : Intron Variant | AD |
rs4321970 | chr8:95093632 | T>A | SNV | NDUFAF6 : Intron Variant | AD |
rs7148434 | chr14:95011422 | A>G | SNV | Intergenic | AD |
rs11107851 | chr12:94995067 | T>C | SNV | NDUFA12 : Intron Variant | ND |
rs7133992 | chr12:94987926 | A>G | SNV | NDUFA12 : Intron Variant | ND |
rs10172167 | chr2:94963293 | T>G | SNV | Intergenic | AD |
rs11165257 | chr1:94836579 | G>T | SNV | SLC44A3 : Intron Variant | AD |
rs12743267 | chr1:94783750 | C>T | SNV | LINC01057 : Intron Variant | AD |
rs9323915 | chr14:94751275 | A>G | SNV | Intergenic | AD |
rs7963894 | chr12:94741247 | G>A | SNV | Intergenic | AD |
rs2896294 | chr14:94740810 | T>C | SNV | Intergenic | AD |
rs7304470 | chr12:94672612 | G>A | SNV | Intergenic | AD |
rs947386 | chr1:94651601 | C>T | SNV | Intergenic | ND |
rs1048048 | chr15:94481531 | T>C | SNV | MCTP2 : 3 Prime UTR Variant | AD |
rs12892340 | chr14:94467839 | G>A | SNV | SERPINA9 : Intron Variant | AD |
rs2180813 | chr14:94461803 | C>T | SNV | LOC105370635 : Non Coding Transcript Variant | ND |
rs1368839 | chr15:94417126 | T>G | SNV | MCTP2 : Intron Variant | AD |
rs10520754 | chr15:94416180 | C>T | SNV | MCTP2 : Intron Variant | AD |
rs9556369 | chr13:94399306 | A>G | SNV | GPC6 : Intron Variant | ND |
rs7696494 | chr4:94364023 | G>A | SNV | Intergenic | AD |
rs7138291 | chr12:94347930 | T>C | SNV | CEP83 : Intron Variant | AD |
rs3743307 | chr15:94341751 | G>A | SNV | MCTP2 : Intron Variant | AD |
rs4761605 | chr12:94335801 | C>T | SNV | CEP83 : Intron Variant | AD |
rs4328383 | chr15:94320608 | T>G | SNV | MCTP2 : Intron Variant | AD |
rs4761601 | chr12:94278226 | G>A | SNV | CEP83 : Intron Variant PLXNC1 : Intron Variant | AD |
rs9360055 | chr6:94230551 | G>A | SNV | Intergenic | ND |
rs9992640 | chr4:94137142 | A>G | SNV | LOC101929210 : Intron Variant | AD |
rs3847794 | chr12:94135049 | A>G | SNV | Intergenic | AD |
rs1036360 | chr12:94059553 | A>G | SNV | Intergenic | ND |
rs7428007 | chr3:93919173 | A>G | SNV | PROS1 : Intron Variant | AD |
rs10464585 | chr7:93806655 | A>G | SNV | Intergenic | AD |
rs7765319 | chr6:93763439 | C>A / C>T | SNV | TSG1 : Intron Variant | AD |
rs13208357 | chr6:93679742 | C>T | SNV | Intergenic | AD |
rs9668896 | chr12:93677236 | C>T | SNV | CRADD : 2KB Upstream Variant | ND |
rs11793637 | chr9:93653617 | A>G / A>T | SNV | PHF2 : Intron Variant | AD |
rs11966981 | chr6:93624202 | G>A | SNV | LOC105377899 : Intron Variant | AD |
rs17021323 | chr12:93579094 | A>G | SNV | SOCS2 : Intron Variant | AD |
rs7126188 | chr11:93544100 | C>T | SNV | SMCO4 : Intron Variant | AD |
rs4847431 | chr1:93519247 | G>A / G>C | SNV | FNBP1L : Intron Variant | ND |
rs12882384 | chr14:93519101 | A>C / A>G | SNV | UNC79 : Intron Variant | ND |
rs11164938 | chr1:93474313 | A>G | SNV | FNBP1L : Intron Variant | AD |
rs625822 | chr6:93403084 | C>T | SNV | EPHA7 : Intron Variant | AD |
rs7060195 | chrX:93398386 | T>G | SNV | Intergenic | AD |
rs2086106 | chr9:93382067 | T>C | SNV | Intergenic | AD |
rs277778 | chr8:93340574 | A>G | SNV | LOC105375642 : Intron Variant LOC107986956 : 2KB Upstream Variant | AD |
rs10882215 | chr10:93304380 | G>T | SNV | Intergenic | AD |
rs1872052 | chr15:93209649 | T>C | SNV | Intergenic | OD |
rs8036747 | chr15:93209226 | G>A | SNV | Intergenic | OD |
rs12442183 | chr15:93204756 | C>T | SNV | LOC105370980 : 2KB Upstream Variant | OD |
rs13285107 | chr9:93118772 | C>T | SNV | Intergenic | AD |
rs1483453 | chr8:93103299 | A>G | SNV | Intergenic | AD |
rs160816 | chr13:93099704 | G>A | SNV | Intergenic | AD |
rs11990542 | chr8:93067757 | G>A | SNV | Intergenic | AD |
rs17437983 | chr6:92965114 | T>C | SNV | Intergenic | AD |
rs7542608 | chr1:92935637 | A>G | SNV | FAM69A : Intron Variant | AD |
rs10493863 | chr1:92934137 | T>C | SNV | FAM69A : Intron Variant | AD |
rs6698233 | chr1:92931743 | C>T | SNV | FAM69A : Intron Variant | AD |
rs737383 | chr11:92931709 | T>C | SNV | Intergenic | ND |
rs7515257 | chr1:92928161 | G>A | SNV | FAM69A : Intron Variant | AD |
rs10241695 | chr7:92913535 | C>T | SNV | LOC101927497 : Intron Variant | AD |
rs2255723 | chr1:92902752 | G>T | SNV | FAM69A : Intron Variant | AD |
rs2263247 | chr1:92898510 | T>C | SNV | FAM69A : Intron Variant | AD |
rs2481713 | chr1:92889332 | G>T | SNV | FAM69A : Intron Variant | AD |
rs2391177 | chr1:92888386 | G>A | SNV | FAM69A : Intron Variant | AD |
rs10782946 | chr1:92887112 | G>A | SNV | FAM69A : Intron Variant | AD |
rs10874744 | chr1:92840760 | G>A | SNV | SNORA66 : Non Coding Transcript Variant FAM69A : Intron Variant RPL5 : Intron Variant | AD |
rs10821008 | chr9:92725215 | G>A | SNV | BICD2 : Intron Variant | AD |
rs10859354 | chr12:92655913 | T>C | SNV | Intergenic | AD |
rs6583832 | chr10:92641615 | T>G | SNV | KIF11 : Intron Variant | ND |
rs6964507 | chr7:92581624 | T>C | SNV | FAM133B : Intron Variant | AD |
rs6465363 | chr7:92577956 | C>T | SNV | FAM133B : Intron Variant | AD |
rs1556562 | chr1:92568466 | G>T | SNV | EVI5 : Intron Variant | AD |
rs4847377 | chr1:92557593 | A>C | SNV | EVI5 : Intron Variant | AD |
rs4735183 | chr8:92556715 | G>T | SNV | Intergenic | AD |
rs2256182 | chr8:92555837 | T>C | SNV | Intergenic | AD |
rs929412 | chr7:92536548 | C>T | SNV | RBM48 : Intron Variant | AD |
rs6603981 | chr1:92528250 | C>T | SNV | EVI5 : Intron Variant | AD |
rs4970712 | chr1:92527990 | A>C | SNV | EVI5 : Intron Variant | AD |
rs1408916 | chr1:92527070 | G>A / G>C | SNV | EVI5 : Intron Variant | AD |
rs6603979 | chr1:92513797 | A>G | SNV | EVI5 : Synonymous Variant | AD |
rs1886682 | chr1:92511718 | A>G / A>T | SNV | EVI5 : 3 Prime UTR Variant | AD |
rs10782922 | chr1:92509038 | G>A | SNV | EVI5 : 3 Prime UTR Variant | AD |
rs4970698 | chr1:92507376 | T>C | SNV | Intergenic | AD |
rs7809455 | chr7:92506759 | T>C | SNV | PEX1 : Intron Variant | AD |
rs3213609 | chr7:92501715 | A>G | SNV | PEX1 : Intron Variant | AD |
rs8040009 | chr15:92501109 | T>C | SNV | C15orf32 : 3 Prime UTR Variant | AD |
rs2031494 | chr1:92500412 | T>C | SNV | Intergenic | AD |
rs6944759 | chr7:92486787 | C>T | SNV | GATAD1 : Intron Variant PEX1 : 500B Downstream Variant | AD |
rs8019291 | chr14:92464820 | G>C / G>T | SNV | SLC24A4 : Intron Variant | ND |
rs10820978 | chr9:92458319 | G>T | SNV | CENPP : Intron Variant ASPN : Intron Variant | AD |
rs2287179 | chr7:92451081 | A>G | SNV | GATAD1 : Intron Variant | AD |
rs4729043 | chr7:92448402 | G>A | SNV | GATAD1 : Intron Variant | AD |
rs2798253 | chr10:92443148 | G>C | SNV | Intergenic | ND |
rs2025607 | chr1:92424787 | C>T | SNV | GLMN : Intron Variant | AD |
rs12740 | chr7:92399988 | G>A | SNV | ANKIB1 : Non Coding Transcript Variant | AD |
rs1906279 | chr1:92350591 | T>C | SNV | RPAP2 : Intron Variant GLMN : Intron Variant | AD |
rs10820967 | chr9:92339447 | G>C | SNV | CENPP : Intron Variant | AD |
rs716623 | chr13:92329669 | A>G | SNV | GPC5 : Intron Variant | ND |
rs6668685 | chr1:92326255 | G>T | SNV | GLMN : Intron Variant RPAP2 : Intron Variant | AD |
rs3103177 | chr1:92290950 | A>G | SNV | GLMN : Intron Variant | AD |
rs1487539 | chr1:92274142 | C>T | SNV | GLMN : Intron Variant | AD |
rs12704637 | chr7:92245372 | C>T | SNV | KRIT1 : Intron Variant ANKIB1 : 2KB Upstream Variant | AD |
rs3122320 | chr1:92240081 | C>T | SNV | C1orf146 : Intron Variant | AD |
rs3131824 | chr1:92224379 | G>A | SNV | C1orf146 : Intron Variant | AD |
rs556155 | chr9:92223355 | T>C | SNV | IARS : Missense Variant | AD |
rs6465353 | chr7:92150657 | T>G | SNV | LRRD1 : Missense Variant CYP51A1-AS1 : Intron Variant | AD |
rs17807815 | chr14:92089711 | T>C | SNV | ATXN3 : Intron Variant | AD |
rs12910142 | chr15:92080273 | G>A | SNV | SLCO3A1 : Intron Variant | ND |
rs7173864 | chr15:92067237 | T>C | SNV | SLCO3A1 : Intron Variant | ND |
rs12536529 | chr7:92054772 | A>G | SNV | AKAP9 : Intron Variant | AD |
rs4932598 | chr15:91994615 | T>C | SNV | SLCO3A1 : Intron Variant LOC107984747 : Non Coding Transcript Variant | ND |
rs4932597 | chr15:91994387 | A>G | SNV | SLCO3A1 : Intron Variant LOC107984747 : Non Coding Transcript Variant | ND |
rs12439765 | chr15:91992372 | C>G | SNV | SLCO3A1 : Intron Variant LOC107984747 : Intron Variant | ND |
rs12439738 | chr15:91992321 | C>T | SNV | SLCO3A1 : Intron Variant LOC107984747 : Intron Variant | ND |
rs7163369 | chr15:91990684 | G>A | SNV | SLCO3A1 : Intron Variant LOC107984747 : Intron Variant | ND |
rs10859259 | chr12:91976430 | C>T | SNV | Intergenic | AD |
rs11106374 | chr12:91974317 | T>C | SNV | Intergenic | AD |
rs7132890 | chr12:91966063 | G>A | SNV | LOC105369901 : Intron Variant | AD |
rs10777366 | chr12:91959975 | C>A | SNV | LOC105369901 : Intron Variant | AD |
rs4542452 | chr12:91945057 | C>A | SNV | LOC105369901 : Intron Variant | AD |
rs10777357 | chr12:91942918 | A>G | SNV | LOC105369901 : Intron Variant | AD |
rs10745574 | chr12:91937812 | A>G | SNV | LOC105369901 : Intron Variant | AD |
rs11106345 | chr12:91932724 | T>C | SNV | LOC105369901 : Intron Variant | AD |
rs4842798 | chr12:91931644 | T>C | SNV | LOC105369901 : Intron Variant | AD |
rs12427267 | chr12:91930196 | A>G | SNV | LOC105369901 : Intron Variant | AD |
rs4499040 | chr12:91928782 | G>A | SNV | LOC105369901 : Intron Variant | AD |
rs4356270 | chr12:91925439 | G>A | SNV | LOC105369901 : Intron Variant | AD |
rs4753350 | chr11:91884381 | A>G | SNV | Intergenic | AD |
rs2489188 | chr1:91866932 | C>T | SNV | TGFBR3 : Intron Variant | AD |
rs7722750 | chr5:91865513 | G>T | SNV | Intergenic | AD |
rs4075845 | chr15:91854794 | T>C | SNV | SLCO3A1 : Intron Variant LOC105370974 : 2KB Upstream Variant | ND |
rs7165398 | chr15:91850865 | T>A / T>C | SNV | LOC105370974 : Intron Variant | ND |
rs16870132 | chr5:91848747 | T>A / T>C | SNV | Intergenic | AD |
rs10057238 | chr5:91834748 | A>G | SNV | Intergenic | AD |
rs4322641 | chr15:91778892 | C>T | SNV | Intergenic | AD |
rs6881283 | chr5:91759840 | C>T | SNV | Intergenic | AD |
rs12516181 | chr5:91743223 | T>C | SNV | Intergenic | AD |
rs4073735 | chr9:91726133 | C>T | SNV | ROR2 : Intron Variant | AD |
rs4743850 | chr9:91700719 | C>A | SNV | LOC105376147 : Intron Variant | ND |
rs12410523 | chr1:91654580 | G>A | SNV | Intergenic | AD |
rs1855065 | chr9:91473095 | T>G | SNV | Intergenic | AD |
rs1591068 | chr9:91463255 | G>A | SNV | Intergenic | AD |
rs10820857 | chr9:91460639 | G>A | SNV | Intergenic | AD |
rs2144363 | chr6:91332186 | A>C | SNV | Intergenic | AD |
rs12180309 | chr6:91209048 | C>T | SNV | Intergenic | AD |
rs803174 | chr7:91165480 | G>A | SNV | CDK14 : Intron Variant | AD |
rs705362 | chr7:91153219 | A>G | SNV | CDK14 : Intron Variant | AD |
rs8026678 | chr15:91018775 | A>G | SNV | VPS33B : Intron Variant | AD |
rs3743445 | chr15:91017952 | C>T | SNV | VPS33B : Intron Variant | AD |
rs4933618 | chr10:90892814 | C>T | SNV | RPP30 : Intron Variant | AD |
rs12259062 | chr10:90850288 | A>G | SNV | HTR7 : Intron Variant | AD |
rs10881838 | chr10:90830476 | A>G | SNV | HTR7 : Intron Variant | AD |
rs11186320 | chr10:90816691 | T>C | SNV | HTR7 : Intron Variant | AD |
rs2042984 | chr9:90810813 | C>T | SNV | SYK : Intron Variant | AD |
rs8012052 | chr14:90781133 | A>G | SNV | TTC7B : Intron Variant | AD |
rs3740046 | chr10:90741711 | C>T | SNV | HTR7 : 3 Prime UTR Variant | AD |
rs2465115 | chr10:90727078 | G>A / G>T | SNV | Intergenic | AD |
rs13134142 | chr4:90721760 | T>G | SNV | CCSER1 : Intron Variant | AD |
rs12133004 | chr1:90709862 | T>C | SNV | Intergenic | AD |
rs17131133 | chr1:90690374 | A>G | SNV | Intergenic | AD |
rs12116456 | chr1:90675639 | G>A | SNV | Intergenic | AD |
rs4735301 | chr8:90276439 | A>G | SNV | LINC00534 : Intron Variant | AD |
rs62313897 | chr4:90215590 | G>A | SNV | CCSER1 : Intron Variant | AD |
rs7149330 | chr14:90169862 | G>A | SNV | KCNK13 : Intron Variant | AD |
rs16882302 | chr6:89964732 | C>T | SNV | BACH2 : Intron Variant | ND |
rs3212369 | chr16:89920352 | A>G | SNV | MC1R : 3 Prime UTR Variant TUBB3 : 2KB Upstream Variant | AD |
rs17016316 | chr4:89876084 | A>G | SNV | Intergenic | ND |
rs6532194 | chr4:89859751 | C>G / C>T | SNV | Intergenic | AD |
rs2293585 | chr16:89822445 | C>T | SNV | SPIRE2 : Intron Variant | AD |
rs9362672 | chr6:89696274 | C>G | SNV | MDN1 : Intron Variant | AD |
rs2390794 | chr1:89660007 | G>A | SNV | LRRC8C : Intron Variant | ND |
rs11984298 | chr7:89640438 | G>T | SNV | Intergenic | AD |
rs6428561 | chr1:89637060 | G>A | SNV | LRRC8C : Intron Variant | ND |
rs10908907 | chr9:89634669 | G>A | SNV | Intergenic | AD |
rs11780016 | chr8:89588871 | A>G | SNV | Intergenic | AD |
rs2888697 | chr7:89396487 | C>A | SNV | Intergenic | AD |
rs10272660 | chr7:89374270 | A>G | SNV | Intergenic | AD |
rs12302525 | chr12:89332648 | C>G | SNV | Intergenic | ND |
rs13294002 | chr9:89291224 | T>G | SNV | LOC105376136 : Intron Variant | AD |
rs4707535 | chr6:89268187 | T>C | SNV | GABRR2 : Intron Variant | AD |
rs10441779 | chr9:89263787 | C>A / C>T | SNV | Intergenic | AD |
rs12341391 | chr9:89233763 | A>G | SNV | Intergenic | AD |
rs13295927 | chr9:89117794 | T>C | SNV | SHC3 : Intron Variant | AD |
rs1331189 | chr9:89105730 | C>T | SNV | SHC3 : Intron Variant | AD |
rs17165697 | chr7:88951002 | G>A | SNV | ZNF804B : Intron Variant | AD |
rs1372325 | chr10:88933812 | T>C | SNV | ACTA2-AS1 : Non Coding Transcript Variant LOC105379869 : 2KB Upstream Variant | AD |
rs8042108 | chr15:88861649 | C>T | SNV | ACAN : Intron Variant | ND |
rs9630453 | chr15:88860691 | A>G | SNV | ACAN : Intron Variant | ND |
rs1391875 | chr11:88714478 | G>C | SNV | GRM5 : Intron Variant | AD |
rs254778 | chr5:88713776 | G>A | SNV | Intergenic | AD |
rs6483362 | chr11:88679283 | A>G | SNV | GRM5 : Intron Variant | AD |
rs10516812 | chr4:88556950 | C>T | SNV | Intergenic | AD |
rs2131068 | chr11:88548038 | T>A | SNV | GRM5 : Intron Variant | ND |
rs3965782 | chr16:88510386 | G>A / G>C | SNV | ZFPM1 : Intron Variant LOC107984890 : Non Coding Transcript Variant | AD |
rs868874 | chr16:88503975 | T>C | SNV | ZFPM1 : Intron Variant | AD |
rs7930237 | chr11:88384794 | A>G | SNV | LOC101929174 : Intron Variant | AD |
rs894290 | chr15:88281450 | A>G | SNV | Intergenic | AD |
rs10868746 | chr9:88281162 | G>A | SNV | Intergenic | AD |
rs11104778 | chr12:88249525 | C>G | SNV | Intergenic | AD |
rs11849247 | chr14:88242159 | T>C | SNV | KCNK10 : Intron Variant | AD |
rs633687 | chr11:88202856 | G>A | SNV | Intergenic | AD |
rs7157457 | chr14:88179513 | C>T | SNV | LOC105370612 : Intron Variant | AD |
rs302665 | chr11:88146459 | A>G | SNV | RAB38 : Intron Variant | AD |
rs12629581 | chr3:88122078 | A>C | SNV | CGGBP1 : Intron Variant ZNF654 : Intron Variant | AD |
rs2970888 | chr2:88112274 | C>A | SNV | SMYD1 : 3 Prime UTR Variant | AD |
rs2970911 | chr2:88096305 | G>A | SNV | SMYD1 : Intron Variant | AD |
rs17755717 | chr15:88081865 | G>A | SNV | NTRK3 : Intron Variant | AD |
rs2471503 | chr12:88069674 | T>C | SNV | CEP290 : Intron Variant | AD |
rs7655182 | chr4:87984751 | G>A | SNV | Intergenic | AD |
rs9636470 | chr2:87866942 | T>C / T>G | SNV | RGPD2 : Intron Variant | ND |
rs9860340 | chr3:87734826 | A>C / A>G | SNV | LOC105377198 : Intron Variant | AD |
rs791887 | chr10:87651797 | T>A / T>C | SNV | Intergenic | AD |
rs1569332 | chr8:87622477 | G>A | SNV | LOC105375626 : Intron Variant | ND |
rs4561856 | chr3:87610971 | G>A / G>C / G>T | SNV | Intergenic | AD |
rs4728701 | chr7:87542737 | A>G | SNV | ABCB1 : Intron Variant | AD |
rs4728699 | chr7:87539433 | C>T | SNV | ABCB1 : Intron Variant | AD |
rs9936994 | chr16:87469209 | G>A | SNV | ZCCHC14 : Intron Variant | ND |
rs428838 | chr8:87468674 | T>C | SNV | Intergenic | AD |
rs7192628 | chr16:87461252 | C>T | SNV | ZCCHC14 : Intron Variant | ND |
rs11648852 | chr16:87460131 | T>C | SNV | ZCCHC14 : Missense Variant | ND |
rs13334632 | chr16:87457213 | T>C | SNV | ZCCHC14 : Intron Variant | ND |
rs12925472 | chr16:87447426 | C>T | SNV | ZCCHC14 : Intron Variant | ND |
rs3748400 | chr16:87412233 | C>T | SNV | ZCCHC14 : Missense Variant | ND |
rs34068017 | chr16:87407443-87407444 | dupC | Indel | ZCCHC14 : Intron Variant | ND |
rs2241617 | chr16:87407442 | T>C | SNV | ZCCHC14 : Intron Variant | ND |
rs3752862 | chr5:87338156 | G>A | SNV | CCNH : Intron Variant RASA1 : Intron Variant | AD |
rs10868555 | chr9:87309983 | C>A | SNV | Intergenic | AD |
rs55996493 | chr13:87264075 | G>A / G>T | SNV | Intergenic | AD |
rs3857487 | chr6:87253970 | A>G | SNV | ZNF292 : Intron Variant | ND |
rs7833568 | chr8:87249563 | T>A / T>C | SNV | CNBD1 : Intron Variant | AD |
rs2336981 | chr8:87243736 | G>A | SNV | CNBD1 : Intron Variant | AD |
rs2880705 | chr13:87201706 | T>C | SNV | Intergenic | AD |
rs17149800 | chr11:87184579 | T>C | SNV | TMEM135 : Intron Variant | AD |
rs4944672 | chr11:87178406 | C>T | SNV | TMEM135 : Intron Variant | AD |
rs1948206 | chr11:87178242 | C>T | SNV | TMEM135 : Intron Variant | AD |
rs9516574 | chr13:87168105 | C>G | SNV | Intergenic | AD |
rs9516565 | chr13:87166282 | G>A | SNV | Intergenic | AD |
rs4129402 | chr13:87156170 | T>C | SNV | Intergenic | AD |
rs2032793 | chr5:87154488 | G>A | SNV | LOC101929380 : Intron Variant | AD |
rs10152646 | chr15:87121159 | C>T | SNV | LOC105370955 : 2KB Upstream Variant | AD |
rs9524641 | chr13:87115606 | G>A | SNV | Intergenic | AD |
rs1004988 | chr5:87115181 | T>G | SNV | MIR4280 : 2KB Upstream Variant | AD |
rs719779 | chr8:87113490 | T>C | SNV | CNBD1 : Intron Variant | AD |
rs993452 | chr13:87109921 | T>C | SNV | Intergenic | AD |
rs9516472 | chr13:87108709 | T>C | SNV | Intergenic | AD |
rs9516471 | chr13:87108612 | G>A | SNV | Intergenic | AD |
rs9524601 | chr13:87106046 | T>A | SNV | Intergenic | AD |
rs9524600 | chr13:87105954 | A>G | SNV | Intergenic | AD |
rs9584247 | chr13:87105048 | G>C | SNV | Intergenic | AD |
rs9516465 | chr13:87103821 | A>C / A>G | SNV | Intergenic | AD |
rs9524595 | chr13:87102823 | C>A | SNV | Intergenic | AD |
rs9524593 | chr13:87102368 | G>T | SNV | Intergenic | AD |
rs9524592 | chr13:87102225 | A>G | SNV | Intergenic | AD |
rs9590055 | chr13:87102125 | G>A | SNV | Intergenic | AD |
rs13378851 | chr13:87100965 | C>T | SNV | Intergenic | AD |
rs9301988 | chr13:87100262 | G>A | SNV | Intergenic | AD |
rs9301987 | chr13:87098856 | A>G | SNV | Intergenic | AD |
rs9516456 | chr13:87097923 | G>A | SNV | Intergenic | AD |
rs1568549 | chr13:87096963 | A>T | SNV | Intergenic | AD |
rs1568548 | chr13:87096798 | G>C | SNV | Intergenic | AD |
rs1568547 | chr13:87096659 | C>T | SNV | Intergenic | AD |
rs9524579 | chr13:87096432 | C>G | SNV | Intergenic | AD |
rs9524576 | chr13:87096072 | G>A | SNV | Intergenic | AD |
rs9524574 | chr13:87095861 | A>C | SNV | Intergenic | AD |
rs9524572 | chr13:87095251 | T>A | SNV | Intergenic | AD |
rs9524571 | chr13:87095211 | G>C | SNV | Intergenic | AD |
rs9301986 | chr13:87094524 | C>T | SNV | Intergenic | AD |
rs9301985 | chr13:87094267 | A>G | SNV | Intergenic | AD |
rs9301984 | chr13:87094112 | T>C | SNV | Intergenic | AD |
rs9516447 | chr13:87093830 | T>A | SNV | Intergenic | AD |
rs9516446 | chr13:87093537 | A>C | SNV | Intergenic | AD |
rs884093 | chr13:87092855 | T>C | SNV | Intergenic | AD |
rs9301982 | chr13:87092050 | T>C | SNV | Intergenic | AD |
rs9301980 | chr13:87091772 | T>A / T>G | SNV | Intergenic | AD |
rs9516435 | chr13:87091321 | A>T | SNV | Intergenic | AD |
rs9516433 | chr13:87090614 | T>C | SNV | Intergenic | AD |
rs9516432 | chr13:87090028 | G>A | SNV | Intergenic | AD |
rs9524539 | chr13:87088873 | T>C | SNV | Intergenic | AD |
rs9524536 | chr13:87088823 | T>C | SNV | Intergenic | AD |
rs9524535 | chr13:87088777 | A>G | SNV | Intergenic | AD |
rs6650324 | chr13:87088170 | T>C | SNV | Intergenic | AD |
rs2880547 | chr13:87088047 | T>C | SNV | Intergenic | AD |
rs9516430 | chr13:87086209 | T>G | SNV | Intergenic | AD |
rs7323320 | chr13:87085592 | A>G | SNV | Intergenic | AD |
rs17149719 | chr11:87084891 | T>C | SNV | TMEM135 : Intron Variant | AD |
rs9516428 | chr13:87084098 | T>C | SNV | Intergenic | AD |
rs9301969 | chr13:87081919 | T>C | SNV | Intergenic | AD |
rs10161716 | chr13:87080135 | C>T | SNV | Intergenic | AD |
rs9516421 | chr13:87079343 | G>T | SNV | Intergenic | AD |
rs2544689 | chr5:87078941 | C>T | SNV | Intergenic | AD |
rs4307816 | chr13:87077997 | A>G | SNV | Intergenic | AD |
rs9524480 | chr13:87072254 | T>G | SNV | Intergenic | AD |
rs9584222 | chr13:87070564 | G>A | SNV | Intergenic | AD |
rs1344791 | chr12:87070497 | C>T | SNV | LOC105369878 : Intron Variant | AD |
rs9584218 | chr13:87070020 | G>C | SNV | Intergenic | AD |
rs9584217 | chr13:87069909 | C>G | SNV | Intergenic | AD |
rs9524441 | chr13:87065933 | A>G | SNV | Intergenic | AD |
rs9516391 | chr13:87065008 | A>C | SNV | Intergenic | AD |
rs9516389 | chr13:87064491 | T>G | SNV | Intergenic | AD |
rs9524431 | chr13:87063973 | A>G | SNV | Intergenic | AD |
rs9516386 | chr13:87063482 | C>G / C>T | SNV | Intergenic | AD |
rs9524429 | chr13:87062938 | C>T | SNV | Intergenic | AD |
rs9524428 | chr13:87062874 | T>A | SNV | Intergenic | AD |
rs9524427 | chr13:87062435 | G>A | SNV | Intergenic | AD |
rs9524405 | chr13:87061179 | T>C | SNV | Intergenic | AD |
rs9516375 | chr13:87057753 | C>T | SNV | Intergenic | AD |
rs7328552 | chr13:87055687 | G>T | SNV | Intergenic | AD |
rs7715840 | chr5:87055061 | A>C | SNV | LOC645261 : Intron Variant | AD |
rs9301944 | chr13:87054090 | G>A | SNV | Intergenic | AD |
rs9524369 | chr13:87053513 | C>T | SNV | Intergenic | AD |
rs17614444 | chr13:87050963 | T>C | SNV | LOC105370301 : Intron Variant | AD |
rs8002837 | chr13:87049018 | T>G | SNV | LOC105370301 : Intron Variant | AD |
rs9524349 | chr13:87048880 | T>C | SNV | LOC105370301 : Intron Variant | AD |
rs1855480 | chr13:87047292 | A>G | SNV | LOC105370301 : Intron Variant | AD |
rs2410729 | chr5:87044070 | G>A | SNV | Intergenic | AD |
rs17614422 | chr13:87042816 | C>A | SNV | LOC105370301 : Intron Variant | AD |
rs9516349 | chr13:87041835 | C>G | SNV | LOC105370301 : Intron Variant | AD |
rs9584183 | chr13:87040024 | T>C | SNV | LOC105370301 : Intron Variant | AD |
rs9584182 | chr13:87040002 | A>G | SNV | LOC105370301 : Intron Variant | AD |
rs7489737 | chr13:87021168 | C>T | SNV | LOC105370301 : Intron Variant | AD |
rs9516305 | chr13:87019012 | G>A | SNV | LOC105370301 : Intron Variant | AD |
rs9524259 | chr13:87018205 | T>G | SNV | LOC105370301 : Intron Variant | AD |
rs1522016 | chr13:87008539 | A>C | SNV | LOC105370301 : Intron Variant | AD |
rs12554360 | chr9:86971425 | C>T | SNV | GAS1RR : Intron Variant | AD |
rs9524032 | chr13:86970122 | C>T | SNV | Intergenic | AD |
rs9523980 | chr13:86956433 | C>T | SNV | Intergenic | AD |
rs9523979 | chr13:86956227 | G>A / G>C | SNV | Intergenic | AD |
rs9523964 | chr13:86954079 | A>G | SNV | Intergenic | AD |
rs9516185 | chr13:86951348 | G>T | SNV | Intergenic | AD |
rs9523907 | chr13:86941307 | G>A | SNV | Intergenic | AD |
rs9523884 | chr13:86932483 | C>A | SNV | LINC00430 : Intron Variant | AD |
rs9523867 | chr13:86927231 | G>A | SNV | LINC00430 : Intron Variant | AD |
rs4526378 | chr8:86922204 | G>T | SNV | CNBD1 : Intron Variant | AD |
rs9523810 | chr13:86914128 | A>C | SNV | LINC00430 : Intron Variant | AD |
rs9523806 | chr13:86909774 | A>G | SNV | LINC00430 : Intron Variant | AD |
rs9523748 | chr13:86896759 | C>T | SNV | Intergenic | AD |
rs7727185 | chr5:86881774 | A>G | SNV | Intergenic | AD |
rs6709175 | chr2:86881088 | T>C | SNV | ANAPC1P1 : Intron Variant | ND |
rs4509845 | chr12:86848345 | A>G | SNV | Intergenic | AD |
rs994029 | chr9:86760399 | C>T | SNV | Intergenic | AD |
rs4961216 | chr8:86748779 | A>C | SNV | Intergenic | AD |
rs6465083 | chr7:86732020 | C>T | SNV | GRM3 : Intron Variant | ND |
rs2237547 | chr7:86718721 | A>C / A>G | SNV | GRM3 : Intron Variant | AD |
rs2189816 | chr7:86712130 | T>C | SNV | GRM3 : Intron Variant | ND |
rs7733888 | chr5:86648119 | T>C | SNV | Intergenic | AD |
rs2362267 | chr8:86614235 | G>A / G>T | SNV | CNGB3 : Intron Variant | ND |
rs1992405 | chr8:86592903 | T>C / T>G | SNV | CNGB3 : Intron Variant | ND |
rs781028 | chr7:86557217 | T>C | SNV | Intergenic | AD |
rs12797615 | chr11:86555641 | T>C | SNV | ME3 : Intron Variant | ND |
rs1321686 | chr1:86508432 | C>T | SNV | Intergenic | ND |
rs1321687 | chr1:86508351 | C>A | SNV | Intergenic | ND |
rs2035985 | chr3:86506819 | C>T | SNV | Intergenic | AD |
rs2791480 | chr1:86502901 | C>G | SNV | LOC105378827 : Non Coding Transcript Variant | ND |
rs1028575 | chr1:86501168 | T>C | SNV | Intergenic | ND |
rs9923190 | chr16:86423027 | C>T | SNV | Intergenic | AD |
rs2103284 | chr16:86413578 | G>A | SNV | Intergenic | AD |
rs12193553 | chr6:86384768 | G>T | SNV | Intergenic | AD |
rs17541873 | chr6:86291852 | G>A | SNV | Intergenic | AD |
rs12437116 | chr14:86225091 | T>C | SNV | Intergenic | AD |
rs220394 | chr6:86175791 | G>A | SNV | Intergenic | AD |
rs9576027 | chr13:86154873 | A>G | SNV | Intergenic | AD |
rs11648147 | chr16:86125764 | A>G | SNV | Intergenic | CD |
rs7867760 | chr9:86113149 | G>C | SNV | Intergenic | AD |
rs1806590 | chr10:86086042 | A>G / A>T | SNV | GRID1 : Intron Variant | ND |
rs9576007 | chr13:86045905 | G>A | SNV | Intergenic | AD |
rs34892520 | chr2:86042040 | C>T | SNV | POLR1A : Missense Variant | CD |
rs7983827 | chr13:86041213 | G>A | SNV | Intergenic | AD |
rs9410906 | chr9:86015871 | C>T | SNV | NAA35 : Intron Variant | AD |
rs17128651 | chr1:86000053 | G>A | SNV | COL24A1 : Intron Variant | AD |
rs511395 | chr9:85947477 | C>T | SNV | NAA35 : Intron Variant | AD |
rs11858797 | chr15:85922484 | T>C | SNV | Intergenic | AD |
rs1999186 | chr1:85619862 | G>A | SNV | Intergenic | AD |
rs4934119 | chr10:85552569 | C>G | SNV | LOC105378404 : Intron Variant | ND |
rs1994074 | chr4:85542405 | T>C | SNV | ARHGAP24 : Intron Variant | AD |
rs9547256 | chr13:85540315 | T>A / T>G | SNV | LINC00351 : Intron Variant | AD |
rs11161614 | chr1:85432477 | T>G | SNV | DDAH1 : Intron Variant | AD |
rs11858860 | chr15:85408215 | T>C | SNV | AKAP13 : Intron Variant | AD |
rs13379803 | chr15:85405478 | C>T | SNV | AKAP13 : Intron Variant | AD |
rs16977810 | chr15:85395420 | C>A / C>G | SNV | AKAP13 : Intron Variant | AD |
rs11752804 | chr6:85318963 | G>A | SNV | Intergenic | AD |
rs13206561 | chr6:85224724 | G>A | SNV | Intergenic | AD |
rs6709476 | chr2:85216801 | G>A | SNV | TCF7L1 : Intron Variant LOC102724579 : Intron Variant | ND |
rs329219 | chr9:85188074 | G>A | SNV | Intergenic | AD |
rs329200 | chr9:85180311 | A>G | SNV | Intergenic | AD |
rs9450148 | chr6:85091002 | A>G | SNV | Intergenic | AD |
rs10118392 | chr9:85065486 | T>C | SNV | Intergenic | CD |
rs1586681 | chr9:85032519 | G>C / G>T | SNV | LOC105376118 : Intron Variant | AD |
rs4877900 | chr9:85017403 | C>T | SNV | NTRK2 : Intron Variant | AD |
rs7026417 | chr9:84974250 | T>C | SNV | NTRK2 : Intron Variant | AD |
rs4980343 | chr15:84928050 | C>A / C>T | SNV | SLC28A1 : Intron Variant | AD |
rs11634491 | chr15:84903829 | A>G | SNV | SLC28A1 : Intron Variant | AD |
rs10868236 | chr9:84893781 | G>T | SNV | NTRK2 : Intron Variant | ND |
rs17078679 | chr13:84882257 | A>G | SNV | LOC105370290 : Intron Variant | AD |
rs1248820 | chr3:84882172 | T>C | SNV | LOC105377192 : Intron Variant | AD |
rs4761097 | chr12:84793732 | G>A | SNV | Intergenic | AD |
rs11576745 | chr1:84774563 | C>T | SNV | Intergenic | AD |
rs12443381 | chr15:84770823 | G>A | SNV | ZNF592 : Intron Variant | AD |
rs1943687 | chr11:84756893 | C>A | SNV | DLG2 : Intron Variant | ND |
rs1940094 | chr11:84698434 | C>T | SNV | DLG2 : Intron Variant | AD |
rs17735215 | chr11:84627241 | T>C | SNV | DLG2 : Intron Variant | ND |
rs11597975 | chr10:84595483 | A>G | SNV | Intergenic | AD |
rs17759625 | chr2:84588560 | A>G | SNV | DNAH6 : Intron Variant | AD |
rs17371334 | chr13:84458192 | T>G | SNV | LINC00333 : Intron Variant LOC105370289 : Intron Variant | ND |
rs17815700 | chr16:84455427 | T>C | SNV | ATP2C2 : Intron Variant | AD |
rs16973814 | chr16:84446014 | G>A / G>T | SNV | ATP2C2 : Intron Variant | AD |
rs17343066 | chr9:84331158 | G>A | SNV | SLC28A3 : Intron Variant | ND |
rs11862438 | chr16:84288047 | C>G | SNV | LOC105376777 : Intron Variant | AD |
rs7845564 | chr8:84206384 | C>T | SNV | RALYL : Intron Variant | AD |
rs153248 | chr5:84174097 | T>C | SNV | EDIL3 : Intron Variant | AD |
rs10261069 | chr7:84172336 | C>T | SNV | SEMA3A : Intron Variant | ND |
rs7808864 | chr7:84094031 | A>G | SNV | SEMA3A : Intron Variant | ND |
rs4943885 | chr11:84055578 | A>G | SNV | DLG2 : Intron Variant | AD |
rs7906877 | chr10:84044036 | C>T | SNV | Intergenic | AD |
rs7076979 | chr10:84043209 | G>A / G>T | SNV | Intergenic | AD |
rs4615965 | chr10:84038824 | C>T | SNV | Intergenic | AD |
rs7068193 | chr10:84035862 | G>A | SNV | Intergenic | AD |
rs6585783 | chr10:84029554 | T>C | SNV | Intergenic | AD |
rs9546566 | chr13:84017727 | A>G | SNV | Intergenic | ND |
rs139438618 | chr7:84008281 | A>G | SNV | SEMA3A : Intron Variant | AD |
rs9546562 | chr13:84001894 | C>A | SNV | Intergenic | ND |
rs3809622 | chr16:83897933 | C>G / C>T | SNV | MLYCD : 2KB Upstream Variant | AD |
rs6885336 | chr5:83865459 | G>A | SNV | Intergenic | AD |
rs11200700 | chr10:83854079 | A>G | SNV | Intergenic | AD |
rs4832336 | chr2:83830839 | G>A / G>C | SNV | Intergenic | AD |
rs7206133 | chr16:83728501 | A>G / A>T | SNV | CDH13 : Intron Variant LOC105371366 : Intron Variant | ND |
rs1563551 | chr5:83726007 | A>G | SNV | Intergenic | AD |
rs877800 | chr14:83725901 | C>T | SNV | Intergenic | AD |
rs419382 | chr16:83725484 | T>C | SNV | CDH13 : Intron Variant LOC105371366 : Non Coding Transcript Variant | ND |
rs9323737 | chr14:83716318 | A>G | SNV | Intergenic | AD |
rs5922858 | chrX:83716000 | G>T | SNV | Intergenic | AD |
rs10873350 | chr14:83714525 | G>A | SNV | Intergenic | AD |
rs1958420 | chr14:83714020 | T>G | SNV | Intergenic | AD |
rs5968205 | chrX:83699482 | C>T | SNV | Intergenic | AD |
rs17688077 | chr16:83622659 | C>T | SNV | CDH13 : Intron Variant | ND |
rs5922838 | chrX:83616187 | A>C / A>G | SNV | Intergenic | AD |
rs4074375 | chr16:83521508 | T>C / T>G | SNV | CDH13 : Intron Variant | ND |
rs12905964 | chr15:83510363 | C>T | SNV | SH3GL3 : Intron Variant | AD |
rs1491579 | chr15:83509927 | T>C | SNV | SH3GL3 : Intron Variant | AD |
rs2247219 | chr7:83438154 | T>G | SNV | SEMA3E : Intron Variant | ND |
rs17284420 | chr5:83417201 | G>C | SNV | Intergenic | ND |
rs9690922 | chr7:83339206 | A>G | SNV | Intergenic | AD |
rs11641255 | chr16:83123538 | C>A / C>G | SNV | CDH13 : Intron Variant | AD |
rs11150542 | chr16:83123514 | G>A | SNV | CDH13 : Intron Variant | AD |
rs28507852 | chr16:83121720 | T>A | SNV | CDH13 : Intron Variant | AD |
rs1143006 | chr17:83048511 | G>A | SNV | B3GNTL1 : Synonymous Variant | AD |
rs73651015 | chr9:82949359 | A>C | SNV | Intergenic | CD |
rs11150518 | chr16:82896123 | G>A | SNV | CDH13 : Intron Variant | ND |
rs6429835 | chr1:82766183 | C>T | SNV | Intergenic | AD |
rs11588936 | chr1:82737456 | T>A | SNV | Intergenic | AD |
rs11588508 | chr1:82737253 | A>G | SNV | Intergenic | AD |
rs1338361 | chr1:82730738 | T>A / T>C | SNV | Intergenic | AD |
rs12500169 | chr4:82723573 | C>G / C>T | SNV | SCD5 : Intron Variant | AD |
rs10493727 | chr1:82723138 | C>T | SNV | Intergenic | AD |
rs12744723 | chr1:82718446 | C>T | SNV | Intergenic | AD |
rs4620789 | chr12:82714616 | G>T | SNV | TMTC2 : Intron Variant | AD |
rs1469743 | chr1:82712497 | G>T | SNV | Intergenic | AD |
rs12579483 | chr12:82695652 | T>C | SNV | TMTC2 : Intron Variant | AD |
rs11640875 | chr16:82687819 | A>G | SNV | CDH13 : Intron Variant MIR8058 : 2KB Upstream Variant | AD |
rs1882582 | chr12:82681935 | G>A | SNV | Intergenic | AD |
rs4254133 | chr12:82677869 | C>T | SNV | Intergenic | AD |
rs1433761 | chr1:82666717 | A>C | SNV | Intergenic | AD |
rs6731289 | chr2:82665670 | C>A | SNV | Intergenic | AD |
rs376096 | chr6:82660735 | T>C | SNV | LOC105377876 : Intron Variant | ND |
rs2787985 | chr1:82652361 | T>G | SNV | LOC105378814 : Intron Variant | AD |
rs453456 | chr1:82651686 | G>A | SNV | LOC105378814 : Intron Variant | AD |
rs373905 | chr1:82647039 | C>T | SNV | LOC105378814 : Intron Variant | AD |
rs12822754 | chr12:82646831 | A>G | SNV | Intergenic | AD |
rs6877560 | chr5:82619482 | A>G | SNV | Intergenic | OD |
rs10121807 | chr9:82521969 | A>G | SNV | LOC107987087 : Intron Variant | ND |
rs1937970 | chr10:82463710 | A>G | SNV | NRG3 : Intron Variant | AD |
rs2429239 | chr5:82440976 | A>C | SNV | Intergenic | OD |
rs224938 | chr5:82421357 | C>T | SNV | Intergenic | OD |
rs17019771 | chr3:82408979 | A>G | SNV | Intergenic | ND |
rs6975142 | chr7:82388133 | A>C / A>T | SNV | CACNA2D1 : Intron Variant | AD |
rs4782727 | chr16:82267442 | A>C / A>T | SNV | Intergenic | AD |
rs12102745 | chr16:82248412 | A>G | SNV | Intergenic | AD |
rs9944350 | chr16:82214277 | A>T | SNV | Intergenic | AD |
rs2967395 | chr16:82199458 | G>C | SNV | Intergenic | AD |
rs929892 | chr16:82198839 | G>A | SNV | Intergenic | AD |
rs2967394 | chr16:82198200 | C>T | SNV | Intergenic | AD |
rs2967393 | chr16:82198064 | T>C | SNV | Intergenic | AD |
rs2911411 | chr16:82197520 | G>A | SNV | Intergenic | AD |
rs2967391 | chr16:82196787 | T>G | SNV | Intergenic | AD |
rs6942458 | chr7:82153198 | A>G | SNV | CACNA2D1 : Intron Variant | ND |
rs13208556 | chr6:82121594 | C>T | SNV | Intergenic | AD |
rs9443958 | chr6:82119121 | C>T | SNV | Intergenic | AD |
rs656948 | chr11:82041701 | C>T | SNV | MIR4300HG : Intron Variant | AD |
rs7961308 | chr12:82010721 | T>C | SNV | Intergenic | AD |
rs1347222 | chr12:82000375 | T>C | SNV | Intergenic | AD |
rs7431326 | chr3:81970452 | G>A | SNV | Intergenic | AD |
rs4580155 | chr16:81968499 | T>C | SNV | Intergenic | AD |
rs4312298 | chr16:81947571 | T>G | SNV | PLCG2 : Intron Variant | AD |
rs7018590 | chr9:81905521 | A>G | SNV | LOC105376108 : Intron Variant | AD |
rs1341260 | chr1:81898976 | T>C | SNV | ADGRL2 : Intron Variant | ND |
rs12676336 | chr8:81858773 | C>T | SNV | Intergenic | AD |
rs28390260 | chr8:81856940 | A>T | SNV | Intergenic | AD |
rs2400540 | chr8:81851713 | A>C | SNV | Intergenic | AD |
rs7839178 | chr8:81851244 | A>G | SNV | Intergenic | AD |
rs1451995 | chr8:81833888 | G>C | SNV | SNX16 : Intron Variant | AD |
rs9972517 | chr15:81826810 | C>T | SNV | Intergenic | AD |
rs4739627 | chr8:81822422 | A>G | SNV | SNX16 : Intron Variant | AD |
rs12544174 | chr8:81819242 | G>A | SNV | SNX16 : Intron Variant | AD |
rs13255262 | chr8:81815789 | T>G | SNV | SNX16 : Intron Variant | AD |
rs6473311 | chr8:81814447 | G>A | SNV | SNX16 : Intron Variant | AD |
rs7825180 | chr8:81811756 | T>A | SNV | SNX16 : Intron Variant | AD |
rs10958045 | chr8:81810759 | T>C | SNV | SNX16 : Intron Variant | AD |
rs7846521 | chr8:81805872 | A>G | SNV | SNX16 : Intron Variant | AD |
rs1054078 | chr8:81799918 | A>G | SNV | SNX16 : 3 Prime UTR Variant | AD |
rs6473310 | chr8:81795746 | A>G / A>T | SNV | Intergenic | AD |
rs6473309 | chr8:81795645 | A>G | SNV | Intergenic | AD |
rs6473308 | chr8:81795473 | G>A | SNV | Intergenic | AD |
rs2400474 | chr8:81794204 | A>G | SNV | Intergenic | AD |
rs10091077 | chr8:81793229 | A>G | SNV | Intergenic | AD |
rs7834483 | chr8:81792593 | A>G | SNV | Intergenic | AD |
rs8043322 | chr15:81792593 | A>C | SNV | Intergenic | AD |
rs7178747 | chr15:81791436 | T>A / T>G | SNV | Intergenic | AD |
rs6415653 | chr8:81790301 | A>C / A>G | SNV | Intergenic | AD |
rs6415652 | chr8:81790022 | G>A | SNV | Intergenic | AD |
rs7835342 | chr8:81785857 | A>G | SNV | Intergenic | AD |
rs7834555 | chr8:81785390 | A>G | SNV | Intergenic | AD |
rs17295389 | chr13:81741664 | G>A | SNV | Intergenic | ND |
rs261446 | chr13:81726846 | T>C | SNV | Intergenic | AD |
rs9593569 | chr13:81567486 | G>A | SNV | LOC105370283 : Intron Variant | AD |
rs2400954 | chr12:81539202 | C>T | SNV | PPFIA2 : Intron Variant | AD |
rs4437240 | chr4:81510915 | C>A / C>G / C>T | SNV | Intergenic | AD |
rs11163319 | chr1:81506757 | A>C | SNV | ADGRL2 : Intron Variant | OD |
rs17582647 | chr8:81372178 | T>C | SNV | Intergenic | ND |
rs510550 | chr10:81368229 | A>G | SNV | Intergenic | AD |
rs7042916 | chr9:81284080 | G>A / G>T | SNV | Intergenic | AD |
rs4889294 | chr16:81270154 | T>C | SNV | BCO1 : Intron Variant | AD |
rs8044334 | chr16:81215330 | T>G | SNV | PKD1L2 : Intron Variant | AD |
rs7733625 | chr5:81086987 | G>T | SNV | RASGRF2 : Intron Variant | AD |
rs16972726 | chr15:81075468 | T>C | SNV | Intergenic | AD |
rs9593517 | chr13:81019942 | A>G | SNV | LINC00377 : Intron Variant | AD |
rs506598 | chr5:81019851 | G>A | SNV | RASGRF2 : Intron Variant | ND |
rs853050 | chr7:80990291 | C>T | SNV | Intergenic | AD |
rs11653325 | chr17:80936829 | T>C | SNV | RPTOR : Intron Variant | ND |
rs10874182 | chr1:80935413 | C>T | SNV | Intergenic | AD |
rs868432 | chr17:80903935 | G>A | SNV | RPTOR : Intron Variant | ND |
rs17019859 | chr2:80898111 | G>A | SNV | Intergenic | ND |
rs6547333 | chr2:80872195 | A>G / A>T | SNV | Intergenic | ND |
rs908241 | chr17:80861878 | G>A / G>T | SNV | RPTOR : Intron Variant | ND |
rs12591074 | chr15:80845525 | C>T | SNV | CEMIP : Intron Variant | AD |
rs2329172 | chr13:80845244 | G>A | SNV | Intergenic | AD |
rs12372944 | chr15:80843108 | T>C | SNV | CEMIP : Intron Variant MIR549A : 2KB Upstream Variant | AD |
rs6874652 | chr5:80834893 | C>T | SNV | MSH3 : Intron Variant | AD |
rs3797898 | chr5:80827492 | C>T | SNV | MSH3 : Intron Variant | AD |
rs6151896 | chr5:80825827 | G>T | SNV | MSH3 : Intron Variant | AD |
rs2306371 | chr5:80813439 | T>C | SNV | MSH3 : Intron Variant | AD |
rs73513496 | chr11:80799224 | A>G | SNV | Intergenic | AD |
rs6547332 | chr2:80791762 | G>A | SNV | Intergenic | ND |
rs9318714 | chr13:80781488 | G>A | SNV | LOC105377818 : Non Coding Transcript Variant | AD |
rs9927571 | chr16:80623069 | G>A / G>T | SNV | CDYL2 : Intron Variant | AD |
rs12448290 | chr16:80621986 | T>G | SNV | CDYL2 : Intron Variant | AD |
rs7605261 | chr2:80544065 | T>G | SNV | CTNNA2 : Intron Variant | AD |
rs13423141 | chr2:80543683 | C>T | SNV | CTNNA2 : Intron Variant | AD |
rs1434075 | chr2:80516069 | G>A | SNV | CTNNA2 : Intron Variant | AD |
rs4238521 | chr15:80503787 | A>G | SNV | ARNT2 : Intron Variant | AD |
rs4778800 | chr15:80487417 | T>G | SNV | ARNT2 : Intron Variant | AD |
rs10455370 | chr6:80331150 | C>T | SNV | BCKDHB : Intron Variant | AD |
rs2867709 | chr4:80329287 | C>A | SNV | C4orf22 : Intron Variant | AD |
rs9352817 | chr6:80316162 | T>G | SNV | BCKDHB : Intron Variant | AD |
rs11826437 | chr11:80305459 | T>A / T>G | SNV | Intergenic | AD |
rs4706834 | chr6:80302888 | G>T | SNV | BCKDHB : Intron Variant | AD |
rs2179842 | chr6:80269336 | T>C | SNV | BCKDHB : Intron Variant | AD |
rs3812121 | chr6:80259010 | A>G | SNV | BCKDHB : Intron Variant | AD |
rs9343977 | chr6:80257284 | C>G / C>T | SNV | BCKDHB : Intron Variant | AD |
rs978814 | chr6:80250195 | C>A | SNV | BCKDHB : Intron Variant | AD |
rs9343974 | chr6:80214928 | A>G | SNV | BCKDHB : Intron Variant | AD |
rs11138552 | chr9:80201820 | C>A | SNV | Intergenic | AD |
rs942381 | chr6:80170433 | T>G | SNV | BCKDHB : Intron Variant | AD |
rs13138779 | chr4:80165919 | G>A | SNV | Intergenic | AD |
rs2789686 | chr10:80155380 | T>C | SNV | ANXA11 : 3 Prime UTR Variant | AD |
rs13102102 | chr4:80152518 | T>C | SNV | Intergenic | AD |
rs12953980 | chr18:80150182 | A>G | SNV | PARD6G-AS1 : Intron Variant | AD |
rs10080237 | chr6:80144753 | T>C | SNV | BCKDHB : Intron Variant | AD |
rs11138516 | chr9:80144587 | C>T | SNV | Intergenic | AD |
rs12513014 | chr4:80140268 | A>G | SNV | Intergenic | AD |
rs2322633 | chr6:80136272 | T>C | SNV | BCKDHB : Intron Variant | AD |
rs2322631 | chr6:80134239 | A>C | SNV | BCKDHB : Intron Variant | AD |
rs4706113 | chr6:80129598 | C>T | SNV | BCKDHB : Intron Variant | AD |
rs1328433 | chr9:80128905 | A>G | SNV | Intergenic | AD |
rs9448894 | chr6:80127536 | G>A / G>T | SNV | BCKDHB : Intron Variant | AD |
rs4437429 | chr6:80118875 | A>G | SNV | BCKDHB : Intron Variant | AD |
rs10512096 | chr9:80115418 | T>C | SNV | Intergenic | AD |
rs971258 | chr9:80114927 | C>T | SNV | Intergenic | AD |
rs2298307 | chr6:80106579 | T>C | SNV | BCKDHB : 2KB Upstream Variant | AD |
rs998023 | chr11:80106208 | A>G | SNV | Intergenic | AD |
rs7453746 | chr6:80100296 | T>G | SNV | Intergenic | AD |
rs55730008 | chr14:80096744 | T>C | SNV | Intergenic | AD |
rs10170918 | chr2:80039771 | A>G | SNV | CTNNA2 : Intron Variant | AD |
rs2889900 | chr9:80026158 | C>G | SNV | LINC01507 : Intron Variant | ND |
rs178462 | chr14:79984592 | C>T | SNV | LOC107984134 : Intron Variant | AD |
rs12953577 | chr18:79956624 | G>A | SNV | Intergenic | AD |
rs62103177 | chr18:79864479 | G>A | SNV | KCNG2 : Intron Variant | OD |
rs2293843 | chr14:79854405 | C>T | SNV | NRXN3 : Intron Variant | AD |
rs4596772 | chrX:79847546 | A>G | SNV | Intergenic | AD |
rs10031299 | chr4:79832638 | T>C | SNV | PCAT4 : Intron Variant | AD |
rs746486 | chr5:79802363 | G>A | SNV | Intergenic | AD |
rs443394 | chr15:79741543 | C>T | SNV | Intergenic | AD |
rs9352760 | chr6:79732196 | G>A | SNV | Intergenic | AD |
rs74641711 | chr18:79727394 | C>T | SNV | CTDP1 : Intron Variant | OD |
rs2463107 | chr12:79699537 | A>C | SNV | Intergenic | AD |
rs1394289 | chr6:79601644 | T>C | SNV | SH3BGRL2 : Intron Variant | AD |
rs2165387 | chr4:79570666 | T>C | SNV | LINC00989 : Intron Variant LOC107986294 : Intron Variant | AD |
rs1415571 | chr15:79527529 | G>T | SNV | Intergenic | AD |
rs11638410 | chr15:79522801 | G>A | SNV | Intergenic | AD |
rs177820 | chr18:79516964 | A>G | SNV | NFATC1 : Intron Variant LOC102723506 : Non Coding Transcript Variant | AD |
rs4778700 | chr15:79495493 | A>G | SNV | Intergenic | AD |
rs12808922 | chr11:79467767 | A>G | SNV | Intergenic | AD |
rs2100290 | chr2:79405221 | A>G | SNV | Intergenic | ND | AD |
rs1609276 | chr7:79299845 | G>C | SNV | MAGI2 : Intron Variant | AD |
rs10504702 | chr8:79299014 | G>A | SNV | Intergenic | AD |
rs12603684 | chr17:79227717 | G>T | SNV | RBFOX3 : Intron Variant | AD |
rs2493600 | chr9:79206176 | C>T | SNV | Intergenic | AD |
rs9352704 | chr6:79200601 | T>C | SNV | Intergenic | AD |
rs8028654 | chr15:79191741 | T>G | SNV | ANKRD34C-AS1 : Non Coding Transcript Variant | AD |
rs630970 | chr11:79013169 | A>T | SNV | TENM4 : Intron Variant | ND |
rs9935088 | chr16:78945618 | A>G | SNV | WWOX : Intron Variant | AD |
rs514463 | chr7:78875415 | G>A | SNV | MAGI2 : Intron Variant | ND |
rs13308578 | chr7:78779243 | C>T | SNV | MAGI2 : Intron Variant | AD |
rs9945493 | chr18:78743253 | G>A | SNV | Intergenic | AD |
rs487651 | chr12:78699457 | T>C / T>G | SNV | Intergenic | AD |
rs6495308 | chr15:78615314 | T>C | SNV | CHRNA3 : Intron Variant | ND |
rs1317286 | chr15:78603787 | A>G | SNV | CHRNA3 : Intron Variant | ND |
rs1051730 | chr15:78601997 | G>A | SNV | CHRNA3 : Synonymous Variant | ND |
rs578776 | chr15:78596058 | G>A | SNV | CHRNA3 : Intron Variant | ND |
rs16969968 | chr15:78590583 | G>A | SNV | CHRNA5 : Missense Variant | ND |
rs951266 | chr15:78586199 | G>A | SNV | CHRNA5 : Intron Variant | ND |
rs569207 | chr15:78580777 | C>T | SNV | CHRNA5 : Intron Variant | ND |
rs680244 | chr15:78578946 | T>C | SNV | CHRNA5 : Intron Variant | ND |
rs9960787 | chr18:78577612 | G>A | SNV | Intergenic | AD |
rs10401125 | chr18:78576288 | C>A / C>T | SNV | Intergenic | AD |
rs1357096 | chr12:78565116 | G>A | SNV | Intergenic | AD |
rs12705591 | chr7:78562053 | T>C | SNV | MAGI2 : Intron Variant | AD |
rs13242509 | chr7:78560896 | T>C | SNV | MAGI2 : Intron Variant | AD |
rs17640190 | chr16:78560010 | G>A / G>C | SNV | WWOX : Intron Variant | ND |
rs12705579 | chr7:78554905 | G>A | SNV | MAGI2 : Intron Variant | AD |
rs13245734 | chr7:78554235 | G>T | SNV | MAGI2 : Intron Variant | AD |
rs34684276 | chr15:78520813 | G>A | SNV | HYKK : Intron Variant | ND |
rs2090836 | chr12:78487730 | C>T | SNV | Intergenic | AD |
rs6466241 | chr7:78475159 | T>C | SNV | MAGI2 : Intron Variant | AD |
rs17484235 | chr15:78469072 | C>A / C>G / C>T | SNV | IREB2 : Intron Variant | ND |
rs2738652 | chr16:78460459 | T>A | SNV | WWOX : Intron Variant | ND |
rs919888 | chr10:78455530 | C>A / C>G | SNV | LOC107984245 : Intron Variant | ND |
rs17405217 | chr15:78438807 | C>G / C>T | SNV | IREB2 : Intron Variant | ND |
rs17483548 | chr15:78437971 | G>A | SNV | IREB2 : 2KB Upstream Variant | ND |
rs17150722 | chr7:78429448 | A>T | SNV | MAGI2 : Intron Variant | ND |
rs12326991 | chr18:78418452 | T>C / T>G | SNV | Intergenic | AD |
rs719871 | chr10:78385678 | C>T | SNV | Intergenic | AD |
rs10490996 | chr10:78371685 | G>A | SNV | Intergenic | AD |
rs11109504 | chr12:78362131 | G>A | SNV | Intergenic | ND |
rs7173851 | chr15:78286317 | T>G | SNV | WDR61 : Intron Variant | AD |
rs1030547 | chr8:78273988 | G>A | SNV | LOC105375911 : Intron Variant | AD |
rs4508428 | chr16:78269369 | T>C | SNV | WWOX : Intron Variant | ND |
rs2071214 | chr17:78223510 | G>A | SNV | BIRC5 : Missense Variant | AD |
rs17754467 | chr14:78156180 | A>G | SNV | NRXN3 : Intron Variant | AD |
rs4903712 | chr14:78149250 | T>C | SNV | NRXN3 : Intron Variant | AD |
rs3823787 | chr7:78143815 | T>C | SNV | MAGI2 : Intron Variant | ND |
rs4798993 | chr18:78124353 | C>T | SNV | Intergenic | AD |
rs10483889 | chr14:78091162 | T>G | SNV | NRXN3 : Intron Variant | AD |
rs4903705 | chr14:78089598 | C>T | SNV | NRXN3 : Intron Variant | AD |
rs11631180 | chr15:78082239 | T>C | SNV | Intergenic | ND |
rs7573381 | chr2:78078496 | A>G | SNV | LOC101927967 : Intron Variant | AD |
rs11126651 | chr2:78077669 | T>G | SNV | LOC101927967 : Intron Variant | AD |
rs12148365 | chr15:78057008 | G>A | SNV | TBC1D2B : Intron Variant | ND |
rs4886554 | chr15:78052580 | G>A | SNV | TBC1D2B : Intron Variant | ND |
rs11873161 | chr18:78026769 | C>T | SNV | Intergenic | AD |
rs9343705 | chr6:77985773 | C>T | SNV | LOC105377865 : Intron Variant | CD |
rs17106558 | chr14:77897589 | G>A | SNV | ADCK1 : Intron Variant | AD |
rs17753195 | chr14:77885419 | G>A | SNV | ADCK1 : Intron Variant | AD |
rs11939576 | chr4:77840844 | A>G | SNV | Intergenic | AD |
rs17002824 | chr4:77837872 | G>A / G>C | SNV | Intergenic | AD |
rs9996218 | chr4:77829346 | A>G | SNV | Intergenic | AD |
rs2866688 | chr4:77827888 | G>A | SNV | Intergenic | AD |
rs6828302 | chr4:77818978 | G>A / G>C | SNV | CNOT6L : Intron Variant | AD |
rs8048150 | chr16:77812766 | T>C | SNV | VAT1L : Intron Variant LOC107984878 : Intron Variant | AD |
rs2812431 | chr10:77789484 | C>T | SNV | Intergenic | AD |
rs2102116 | chr4:77751014 | C>T | SNV | CNOT6L : Intron Variant | AD |
rs7761742 | chr6:77710715 | T>C | SNV | MEI4 : Intron Variant | OD |
rs10871341 | chr16:77709280 | A>G | SNV | Intergenic | AD |
rs35216166 | chr7:77698016 | G>A | SNV | RSBN1L : Intron Variant APTR : 2KB Upstream Variant | AD |
rs9807163 | chr18:77687439 | C>A | SNV | Intergenic | AD |
rs12898370 | chr15:77516256 | A>C / A>T | SNV | HMG20A : Intron Variant | AD |
rs3825694 | chr14:77468244 | T>C | SNV | AHSA1 : Intron Variant | ND |
rs4489889 | chr13:77451851 | C>T | SNV | Intergenic | AD |
rs1343485 | chr6:77451216 | A>C | SNV | LOC105377864 : Intron Variant | AD |
rs12131772 | chr1:77417986 | C>G | SNV | AK5 : Intron Variant | ND |
rs10873937 | chr1:77414142 | C>T | SNV | AK5 : Intron Variant | ND |
rs12219105 | chr10:77413782 | T>C | SNV | KCNMA1 : Intron Variant | AD |
rs13259667 | chr8:77413649 | G>A | SNV | LOC105375909 : Intron Variant | AD |
rs13258743 | chr8:77413400 | G>A | SNV | LOC105375909 : Intron Variant | AD |
rs4761378 | chr12:77412906 | T>C | SNV | Intergenic | AD |
rs11145410 | chr9:77397484 | G>A | SNV | VPS13A : Intron Variant | ND |
rs2077641 | chr10:77386358 | G>A / G>C / G>T | SNV | KCNMA1 : Intron Variant | AD |
rs11643269 | chr16:77343670 | G>A | SNV | ADAMTS18 : Intron Variant | AD |
rs2411109 | chr17:77336374 | G>A | SNV | SEPT9 : Intron Variant | AD |
rs12380218 | chr9:77320744 | A>G | SNV | VPS13A : Intron Variant | ND |
rs4788985 | chr17:77317253 | A>G | SNV | SEPT9 : Intron Variant | ND | AD |
rs1944550 | chr18:77303607 | A>C / A>G | SNV | Intergenic | AD |
rs11145381 | chr9:77300225 | T>C | SNV | VPS13A : Intron Variant | ND |
rs592676 | chr10:77294199 | T>A | SNV | KCNMA1 : Intron Variant | ND |
rs717207 | chr10:77283606 | G>T | SNV | KCNMA1 : Intron Variant | AD |
rs2022443 | chr9:77254936 | T>G | SNV | VPS13A : Intron Variant | ND |
rs2287386 | chr14:77252278 | C>A | SNV | TMEM63C : Intron Variant | ND |
rs6740940 | chr2:77234761 | C>T | SNV | LRRTM4 : Intron Variant | CD |
rs12680810 | chr8:77231908 | T>A | SNV | Intergenic | ND |
rs12964446 | chr18:77221047 | A>C | SNV | Intergenic | AD |
rs10869910 | chr9:77209086 | C>T | SNV | VPS13A : Intron Variant | ND |
rs11640619 | chr16:77199271 | G>A | SNV | MON1B : 3 Prime UTR Variant SYCE1L : 2KB Upstream Variant | AD |
rs10858504 | chr12:77197636 | T>G | SNV | Intergenic | AD |
rs7821178 | chr8:77181601 | C>A / C>G / C>T | SNV | Intergenic | AD |
rs10824494 | chr10:77158539 | C>A / C>G | SNV | KCNMA1 : Intron Variant | AD |
rs10869902 | chr9:77157174 | G>A | SNV | Intergenic | ND |
rs4142603 | chr9:77154478 | T>C | SNV | Intergenic | ND |
rs2053568 | chr17:77113218 | T>C | SNV | SEC14L1 : Intron Variant LOC105371900 : Intron Variant | AD |
rs7404856 | chr16:77096442 | A>C | SNV | Intergenic | AD |
rs10506725 | chr12:77055734 | T>C | SNV | E2F7 : Intron Variant | AD |
rs679210 | chr17:77049901 | A>C | SNV | Intergenic | AD |
rs4944137 | chr11:77047545 | G>C | SNV | LOC105369399 : 2KB Upstream Variant | AD |
rs2411042 | chr17:76917855 | G>T | SNV | MGAT5B : Intron Variant | AD |
rs562832 | chr18:76915143 | C>T | SNV | ZNF236 : Intron Variant | AD |
rs904050 | chr4:76904936 | T>G | SNV | LOC107986291 : Intron Variant | ND |
rs2703126 | chr4:76898689 | T>C | SNV | SOWAHB : 2KB Upstream Variant LOC107986291 : Intron Variant | ND |
rs936498 | chr6:76820190 | G>A | SNV | LOC105377862 : Non Coding Transcript Variant | AD |
rs6565917 | chr18:76779719 | A>G | SNV | Intergenic | AD |
rs7127747 | chr11:76701619 | G>A | SNV | GUCY2EP : Intron Variant | AD |
rs17200717 | chr12:76683318 | T>C | SNV | Intergenic | AD |
rs16939329 | chr8:76651943 | G>A / G>C | SNV | ZFHX4-AS1 : Intron Variant | ND |
rs10504631 | chr8:76626252 | A>G | SNV | ZFHX4-AS1 : Intron Variant | ND |
rs7046144 | chr9:76616633 | C>T | SNV | PRUNE2 : Intron Variant LOC105376095 : Intron Variant | ND |
rs433780 | chr13:76490896 | C>T | SNV | LOC105370263 : Intron Variant | AD |
rs493863 | chr13:76489395 | A>G | SNV | LOC105370263 : Intron Variant | AD |
rs10942782 | chr5:76485465 | T>C | SNV | IQGAP2 : Intron Variant | AD |
rs12562911 | chr1:76356915 | A>G | SNV | ST6GALNAC3 : Intron Variant | AD |
rs2554840 | chr18:76316449 | A>G | SNV | LOC105372211 : Intron Variant | AD |
rs929853 | chr16:76300776 | G>A | SNV | CNTNAP4 : Intron Variant | AD |
rs10762705 | chr10:76268705 | G>A | SNV | C10orf11 : Intron Variant | AD |
rs10899187 | chr11:76255283 | T>C | SNV | Intergenic | AD |
rs2226615 | chr11:76245304 | G>A | SNV | Intergenic | AD |
rs2447947 | chr11:76232496 | T>C | SNV | Intergenic | AD |
rs2866619 | chr16:76218244 | G>A | SNV | Intergenic | ND |
rs7024200 | chr9:76078316 | A>G | SNV | PCSK5 : Intron Variant | ND |
rs1030565 | chr18:76051715 | A>C / A>T | SNV | Intergenic | AD |
rs4891112 | chr18:76046148 | G>A | SNV | Intergenic | AD |
rs2792224 | chr9:76042814 | A>G | SNV | PCSK5 : Intron Variant | ND |
rs7297654 | chr12:76019714 | G>A | SNV | Intergenic | ND |
rs4416887 | chr9:75982309 | A>G / A>T | SNV | PCSK5 : Intron Variant | ND |
rs3860052 | chr12:75958919 | T>G | SNV | Intergenic | AD |
rs1538901 | chr13:75942758 | T>C | SNV | Intergenic | AD |
rs16943694 | chr16:75932872 | T>G | SNV | Intergenic | AD |
rs3911770 | chr8:75899473 | T>G | SNV | Intergenic | AD |
rs7314267 | chr12:75898108 | G>A | SNV | Intergenic | AD |
rs1623319 | chr12:75876976 | G>A | SNV | Intergenic | AD |
rs2612391 | chr18:75843162 | G>A / G>T | SNV | Intergenic | AD |
rs2977343 | chr8:75814512 | C>G | SNV | Intergenic | ND |
rs5745331 | chr1:75807628 | A>G | SNV | MSH4 : Intron Variant | AD |
rs4885322 | chr13:75597195 | A>G | SNV | UCHL3 : Intron Variant | ND |
rs237238 | chr7:75582098 | A>C / A>G / A>T | SNV | HIP1 : Synonymous Variant | AD |
rs237240 | chr7:75581343 | C>T | SNV | HIP1 : Intron Variant | AD |
rs11144480 | chr9:75543369 | G>A | SNV | Intergenic | AD |
rs516609 | chr9:75454763 | C>A / C>G / C>T | SNV | Intergenic | AD |
rs3018100 | chr11:75417295 | C>G | SNV | RPS3 : Intron Variant | AD |
rs12267051 | chr10:75346879 | C>G / C>T | SNV | ZNF503 : Intron Variant ZNF503-AS1 : Intron Variant | AD |
rs79749241 | chr8:75290351 | G>A | SNV | Intergenic | CD |
rs512797 | chr11:75285037 | G>A | SNV | ARRB1 : Intron Variant | AD |
rs1468900 | chr2:75222857 | A>G | SNV | LOC105374811 : Intron Variant | AD |
rs17803126 | chr12:75183086 | T>C | SNV | KCNC2 : Intron Variant | ND |
rs10054860 | chr5:75150979 | T>G | SNV | ANKRD31 : Intron Variant | CD |
rs7172677 | chr15:75132252 | A>C | SNV | Intergenic | AD |
rs4479194 | chr15:75129790 | G>A | SNV | Intergenic | AD |
rs2029519 | chr15:75123621 | A>G | SNV | Intergenic | AD |
rs961098 | chr5:75104561 | G>A / G>C | SNV | ANKRD31 : Missense Variant | CD |
rs62059203 | chr16:75098967 | G>C | SNV | ZNRF1 : Intron Variant | CD |
rs2376397 | chr9:75075833 | C>T | SNV | NMRK1 : Intron Variant | AD |
rs4626318 | chr5:75069932 | A>C | SNV | ANKRD31 : Intron Variant | CD |
rs10879871 | chr12:74986731 | T>G | SNV | Intergenic | AD |
rs1560784 | chr8:74891301 | A>C | SNV | Intergenic | AD |
rs2570148 | chr8:74887214 | A>G | SNV | Intergenic | AD |
rs2570147 | chr8:74886626 | T>C | SNV | Intergenic | AD |
rs3732300 | chr2:74872254 | T>C | SNV | HK2 : Intron Variant | ND |
rs690307 | chr17:74863587 | A>C / A>T | SNV | FDXR : Intron Variant | AD |
rs690371 | chr17:74862956 | G>A | SNV | FDXR : Intron Variant | AD |
rs2683267 | chr17:74858860 | C>T | SNV | GRIN2C : Intron Variant | AD |
rs690578 | chr17:74857308 | A>G | SNV | GRIN2C : Intron Variant | AD |
rs690533 | chr17:74854034 | G>A | SNV | GRIN2C : Intron Variant | AD |
rs11652088 | chr17:74843693 | G>A | SNV | GRIN2C : Intron Variant | AD |
rs9901283 | chr17:74841693 | G>A | SNV | GRIN2C : 500B Downstream Variant | AD |
rs1568447 | chr17:74840873 | C>T | SNV | Intergenic | AD |
rs11918452 | chr3:74833134 | G>A | SNV | LOC105377167 : Intron Variant | AD |
rs1918392 | chr3:74831706 | A>G | SNV | LOC105377167 : Intron Variant | AD |
rs16978197 | chr17:74812508 | C>T | SNV | TMEM104 : Intron Variant | AD |
rs12956780 | chr18:74792062 | G>A | SNV | ZNF407 : Intron Variant | AD |
rs7229235 | chr18:74783036 | G>A | SNV | ZNF407 : Intron Variant | AD |
rs1974956 | chr18:74782885 | G>A | SNV | ZNF407 : Intron Variant | AD |
rs7228438 | chr18:74781358 | G>T | SNV | ZNF407 : Intron Variant | AD |
rs7228254 | chr18:74781205 | G>C | SNV | ZNF407 : Intron Variant | AD |
rs9947276 | chr18:74780733 | A>T | SNV | ZNF407 : Intron Variant | AD |
rs10824233 | chr10:74745813 | G>A | SNV | Intergenic | AD |
rs2502521 | chr6:74699718 | T>C | SNV | LOC105377858 : Intron Variant | ND |
rs16978166 | chr17:74677410 | G>A | SNV | RAB37 : Intron Variant LOC105371894 : 2KB Upstream Variant | AD |
rs34158545 | chr7:74586566 | C>G | SNV | GTF2IRD1 : Intron Variant | AD |
rs13246861 | chr7:74586525 | A>G | SNV | GTF2IRD1 : Intron Variant | AD |
rs13244286 | chr7:74586350 | G>A | SNV | GTF2IRD1 : Intron Variant | AD |
rs13293006 | chr9:74521980 | C>A | SNV | RORB : Intron Variant | ND |
rs10869409 | chr9:74508473 | T>C | SNV | RORB : Intron Variant | ND |
rs7846903 | chr9:74500195 | G>A | SNV | RORB : Intron Variant RORB-AS1 : 2KB Upstream Variant | ND |
rs6874566 | chr5:74491055 | T>C | SNV | LINC01331 : Intron Variant | AD |
rs12800641 | chr11:74442195 | G>A | SNV | Intergenic | ND |
rs6472851 | chr8:74426395 | C>G | SNV | GDAP1 : Intron Variant | ND |
rs9897184 | chr17:74418622 | G>A | SNV | Intergenic | AD |
rs7819969 | chr8:74404008 | C>A / C>G | SNV | GDAP1 : Intron Variant | ND |
rs12956327 | chr18:74394359 | G>C / G>T | SNV | Intergenic | CD |
rs658126 | chr11:74388847 | T>A / T>C | SNV | PGM2L1 : Intron Variant | ND |
rs7813767 | chr8:74385107 | G>A | SNV | GDAP1 : Intron Variant | ND |
rs4310196 | chr8:74360492 | C>A | SNV | GDAP1 : Intron Variant | ND |
rs7846006 | chr8:74359739 | A>G | SNV | GDAP1 : Intron Variant | ND |
rs9298238 | chr8:74355383 | A>G | SNV | GDAP1 : Intron Variant | ND |
rs10504567 | chr8:74264853 | G>C | SNV | JPH1 : Intron Variant | AD |
rs17337083 | chr8:74242632 | T>C | SNV | JPH1 : Intron Variant | AD |
rs12457387 | chr18:74224753 | C>G / C>T | SNV | Intergenic | CD |
rs292203 | chr5:74210959 | C>G / C>T | SNV | Intergenic | AD |
rs158810 | chr5:74210286 | T>C | SNV | Intergenic | AD |
rs17591292 | chr1:74180374 | C>T | SNV | LRRIQ3 : Intron Variant | AD |
rs223002 | chr7:74169373 | G>A / G>T | SNV | Intergenic | AD |
rs223011 | chr7:74167072 | C>T | SNV | Intergenic | AD |
rs7775575 | chr6:74148740 | C>T | SNV | LOC101928516 : Intron Variant | AD |
rs288864 | chr5:74132218 | A>G | SNV | Intergenic | AD |
rs2875670 | chr13:73964931 | A>G | SNV | KLF12 : Intron Variant | AD |
rs9318238 | chr13:73963883 | T>C | SNV | KLF12 : Intron Variant | AD |
rs9318232 | chr13:73956142 | T>C | SNV | KLF12 : Intron Variant | AD |
rs2886920 | chr4:73761228 | C>T | SNV | Intergenic | AD |
rs9425128 | chr1:73703600 | C>T | SNV | Intergenic | AD |
rs642490 | chr11:73654570 | A>G | SNV | PLEKHB1 : Intron Variant | AD |
rs1858030 | chr17:73626530 | G>A | SNV | SDK2 : Intron Variant | ND |
rs157113 | chr9:73572623 | T>C | SNV | LOC105376085 : 2KB Upstream Variant | AD |
rs12632758 | chr3:73499249 | C>T | SNV | PDZRN3 : Intron Variant | AD |
rs12632755 | chr3:73499184 | C>T | SNV | PDZRN3 : Intron Variant | AD |
rs11000671 | chr10:73480219 | C>T | SNV | PPP3CB : Intron Variant | ND |
rs3816831 | chr3:73401047 | G>A | SNV | PDZRN3 : Intron Variant | AD |
rs1790063 | chr11:73284867 | G>A | SNV | P2RY6 : Intron Variant | AD |
rs3188114 | chr2:73227128 | G>A | SNV | SMYD5 : 3 Prime UTR Variant | ND |
rs7111814 | chr11:73224780 | C>T | SNV | P2RY2 : Intron Variant | AD |
rs2303904 | chr2:73220647 | A>C / A>G | SNV | SMYD5 : Intron Variant | ND |
rs12662682 | chr6:73180074 | A>G | SNV | KCNQ5 : Intron Variant | AD |
rs1037260 | chr17:73161126 | G>T | SNV | Intergenic | AD |
rs4969069 | chr17:73134434 | C>T | SNV | Intergenic | AD |
rs9835056 | chr3:73130169 | T>C | SNV | LOC107986098 : Intron Variant | AD |
rs4694155 | chr4:73065809 | T>G | SNV | COX18 : Intron Variant | AD |
rs9824246 | chr3:73053574 | A>G | SNV | PPP4R2 : Intron Variant | ND |
rs7085141 | chr10:73017023 | A>G | SNV | P4HA1 : Intron Variant | AD |
rs16930262 | chr10:73007937 | C>T | SNV | P4HA1 : 3 Prime UTR Variant | AD |
rs12573768 | chr10:73004316 | G>A | SNV | Intergenic | AD |
rs885247 | chr6:72950511 | T>C | SNV | KCNQ5 : Intron Variant LOC105377855 : Intron Variant | AD |
rs13251382 | chr8:72922542 | A>G / A>T | SNV | KCNB2 : Intron Variant | AD |
rs2128158 | chr8:72917865 | G>A / G>C / G>T | SNV | KCNB2 : Intron Variant | AD |
rs7120605 | chr11:72733570 | A>G | SNV | ARAP1 : Intron Variant | AD |
rs36057641 | chr15:72730279-72730292 | delAA / delA | Indel | BBS4 : Intron Variant | AD |
rs10515153 | chr5:72693323 | T>C | SNV | Intergenic | AD |
rs11179306 | chr12:72653857 | C>A | SNV | TRHDE : Intron Variant | AD |
rs923572 | chr3:72647860 | G>A | SNV | LOC105377161 : Intron Variant | AD |
rs2526919 | chr14:72641063 | A>G | SNV | DPF3 : Intron Variant | AD |
rs9442829 | chr6:72615796 | A>G | SNV | Intergenic | CD |
rs2803953 | chr14:72604795 | C>A / C>T | SNV | RGS6 : Intron Variant | AD |
rs1490504 | chr3:72601204 | G>A / G>C | SNV | LOC105377161 : Intron Variant | ND |
rs10049135 | chr3:72599829 | A>G | SNV | LOC105377161 : Intron Variant | ND |
rs1446891 | chr2:72579122 | C>T | SNV | EXOC6B : Intron Variant | AD |
rs1446890 | chr2:72568601 | G>A | SNV | EXOC6B : Intron Variant | AD |
rs12471136 | chr2:72562188 | A>G | SNV | EXOC6B : Intron Variant | AD |
rs1431659 | chr8:72526835 | A>G | SNV | LOC105375897 : Intron Variant | AD |
rs2138683 | chr2:72508380 | G>A | SNV | EXOC6B : Intron Variant | AD |
rs11126370 | chr2:72498818 | G>A | SNV | EXOC6B : Intron Variant | AD |
rs10511022 | chr3:72495045 | C>T | SNV | Intergenic | ND |
rs7809631 | chr7:72443666 | G>A / G>T | SNV | CALN1 : Intron Variant | ND |
rs7159300 | chr14:72417166 | G>A / G>T | SNV | RGS6 : Intron Variant LOC105370559 : Intron Variant | ND |
rs11158954 | chr14:72415689 | C>T | SNV | RGS6 : Intron Variant LOC105370559 : Intron Variant | AD |
rs7222185 | chr17:72389426 | G>A / G>C | SNV | Intergenic | AD |
rs2959930 | chr15:72306273 | G>A | SNV | CELF6 : Intron Variant | AD |
rs1157072 | chr1:72169229 | A>G | SNV | NEGR1 : Intron Variant | ND |
rs1024826 | chr17:72151440 | T>C | SNV | Intergenic | AD |
rs10511997 | chr9:72145640 | G>A | SNV | GDA : Intron Variant | AD |
rs9836943 | chr3:72109884 | T>G | SNV | Intergenic | AD |
rs9832693 | chr3:72109759 | A>G | SNV | Intergenic | AD |
rs4677086 | chr3:72109181 | C>G | SNV | Intergenic | AD |
rs1580953 | chr3:72105684 | T>A | SNV | Intergenic | AD |
rs35794819 | chr16:72096204 | C>G | SNV | DHX38 : Missense Variant TXNL4B : 2KB Upstream Variant | AD |
rs17085505 | chr18:72076229 | A>C / A>T | SNV | Intergenic | ND |
rs9860628 | chr3:71993849 | C>T | SNV | LOC105377157 : Intron Variant | AD |
rs7086629 | chr10:71969470 | T>C | SNV | CHST3 : Intron Variant | CD |
rs4747204 | chr10:71839132 | A>G | SNV | PSAP : Intron Variant | AD |
rs2854992 | chr10:71826828 | A>G | SNV | PSAP : Intron Variant | AD |
rs4738159 | chr8:71772166 | C>T | SNV | Intergenic | AD |
rs17088471 | chr13:71768304 | C>A | SNV | DACH1 : Intron Variant | AD |
rs1010434 | chr9:71710517 | C>T | SNV | TMEM2 : Intron Variant | AD |
rs10823825 | chr10:71694880 | T>C | SNV | CDH23 : Intron Variant | AD |
rs10999882 | chr10:71566583 | C>T | SNV | CDH23 : Intron Variant | AD |
rs11158907 | chr14:71520348 | A>G | SNV | SIPA1L1 : Intron Variant | AD |
rs10999845 | chr10:71480604 | A>G | SNV | CDH23 : Intron Variant | ND |
rs12102112 | chr15:71363396 | C>T | SNV | THSD4 : Intron Variant | AD |
rs11209757 | chr1:71263217 | T>A / T>G | SNV | Intergenic | AD |
rs12131265 | chr1:71246540 | C>T | SNV | Intergenic | AD |
rs12766963 | chr10:71236477 | C>G / C>T | SNV | UNC5B : Intron Variant | AD |
rs2042423 | chr16:71201086 | C>T | SNV | HYDIN : Intron Variant | AD |
rs2198341 | chr4:71197327 | G>A | SNV | SLC4A4 : Intron Variant | AD |
rs8016108 | chr14:71187404 | C>T | SNV | LOC107984695 : Intron Variant | AD |
rs17689531 | chr4:71157058 | T>C | SNV | Intergenic | AD |
rs3924047 | chr11:71118812 | T>C | SNV | SHANK2 : Intron Variant | AD |
rs809164 | chr13:71055978 | T>A / T>C / T>G | SNV | LINC00348 : Intron Variant | AD |
rs11238042 | chr11:70942895 | G>A | SNV | SHANK2 : Intron Variant | AD |
rs2810114 | chr14:70928887 | C>A | SNV | PCNX1 : Intron Variant | AD |
rs827330 | chr10:70917835 | A>C | SNV | Intergenic | ND |
rs36563 | chr14:70885931 | T>G | SNV | Intergenic | AD |
rs12229663 | chr12:70856216 | A>G / A>T | SNV | PTPRR : Intron Variant | AD |
rs2769490 | chr13:70794838 | T>C | SNV | LOC105370255 : Intron Variant | AD |
rs2769493 | chr13:70784055 | G>A | SNV | LOC105370255 : Intron Variant | AD |
rs4471563 | chr13:70772187 | T>C | SNV | LOC105370255 : Intron Variant | AD |
rs6562646 | chr13:70769146 | C>A | SNV | LOC105370255 : Intron Variant | AD |
rs12775317 | chr10:70702527 | G>A | SNV | ADAMTS14 : Intron Variant | AD |
rs7940843 | chr11:70680240 | T>C | SNV | SHANK2 : Intron Variant | AD |
rs10257489 | chr7:70672131 | A>C / A>G / A>T | SNV | AUTS2 : Intron Variant | ND |
rs1495858 | chr13:70668635 | G>A | SNV | Intergenic | AD |
rs2107942 | chr7:70666837 | T>C | SNV | AUTS2 : Intron Variant | AD |
rs2465810 | chr12:70621500 | A>G | SNV | PTPRB : Intron Variant | ND |
rs10114679 | chr9:70609644 | C>T | SNV | TRPM3 : Intron Variant | AD |
rs11604385 | chr11:70574867 | C>T | SNV | SHANK2 : Intron Variant | AD |
rs9529776 | chr13:70563016 | G>A | SNV | Intergenic | AD |
rs9542387 | chr13:70562011 | G>A | SNV | Intergenic | AD |
rs17082721 | chr18:70499885 | G>A | SNV | LOC105376872 : Intron Variant | ND |
rs17568303 | chr7:70488924 | C>G | SNV | AUTS2 : Intron Variant | ND |
rs6600832 | chr4:70487791 | C>T | SNV | Intergenic | AD |
rs1109501 | chr4:70463773 | G>A | SNV | MUC7 : Intron Variant | AD |
rs12561944 | chr1:70444382 | A>G | SNV | Intergenic | AD |
rs664051 | chr1:70403433 | G>A | SNV | Intergenic | AD |
rs7317253 | chr13:70395170 | T>G | SNV | Intergenic | AD |
rs17086945 | chr13:70373933 | T>C | SNV | Intergenic | AD |
rs6943555 | chr7:70341037 | T>A | SNV | AUTS2 : Intron Variant | AD |
rs717360 | chr4:70324584 | C>T | SNV | Intergenic | AD |
rs11947897 | chr4:70320004 | C>A | SNV | Intergenic | AD |
rs7242186 | chr18:70314625 | G>A | SNV | SOCS6 : Intron Variant | AD |
rs12698891 | chr7:70300519 | A>G | SNV | AUTS2 : Intron Variant | ND |
rs729314 | chr4:70299989 | C>A / C>T | SNV | Intergenic | AD |
rs11178177 | chr12:70297525 | C>T | SNV | CNOT2 : Intron Variant | AD |
rs2877626 | chr14:70288090 | A>G | SNV | LOC101928046 : Intron Variant | AD |
rs3843841 | chrX:70265679 | A>C | SNV | Intergenic | AD |
rs7175167 | chr15:70233320 | C>T | SNV | Intergenic | AD |
rs16954296 | chr15:70225369 | C>T | SNV | Intergenic | AD |
rs10162898 | chr15:70198164 | G>A | SNV | Intergenic | AD |
rs2009403 | chr15:70185565 | A>G | SNV | Intergenic | AD |
rs8040467 | chr15:70160606 | A>C | SNV | Intergenic | AD |
rs1036536 | chr12:70117766 | C>T | SNV | Intergenic | AD |
rs4902778 | chr14:70113519 | C>T | SNV | SLC8A3 : Intron Variant | AD |
rs1035717 | chr14:70111982 | A>G | SNV | SLC8A3 : Intron Variant | AD |
rs755016 | chr11:70106456 | G>A | SNV | ANO1 : Intron Variant | AD |
rs16936661 | chr8:70058383 | T>C | SNV | PRDM14 : Intron Variant | AD |
rs180172 | chr17:70041173 | A>G | SNV | LOC107983956 : Intron Variant | AD |
rs942568 | chr10:69897865 | G>T | SNV | COL13A1 : Intron Variant | ND |
rs7227328 | chr18:69822648 | G>A / G>C | SNV | DOK6 : Intron Variant | ND |
rs77114337 | chr4:69758944 | T>C | SNV | SULT1B1 : Intron Variant | ND |
rs10241485 | chr7:69742332 | A>G | SNV | AUTS2 : Intron Variant | ND |
rs11151527 | chr18:69679897 | A>G | SNV | DOK6 : Intron Variant | ND |
rs10500553 | chr16:69651111 | A>G | SNV | NFAT5 : Intron Variant | AD |
rs16936012 | chr8:69530638 | G>A / G>T | SNV | SULF1 : Intron Variant | AD |
rs112196420 | chr3:69450652 | G>A / G>T | SNV | FRMD4B : Intron Variant | AD |
rs7312976 | chr12:69442845 | T>C | SNV | Intergenic | CD |
rs1800973 | chr12:69350234 | C>A | SNV | LYZ : Missense Variant | AD |
rs11647864 | chr16:69321603 | C>T | SNV | VPS4A : Intron Variant | AD |
rs13066342 | chr3:69320145 | C>A | SNV | FRMD4B : Intron Variant | ND |
rs7336505 | chr13:69281476 | T>C | SNV | LINC00383 : Intron Variant | ND |
rs12086324 | chr1:69215507 | C>T | SNV | LOC105378786 : Non Coding Transcript Variant LOC105378787 : Intron Variant | AD |
rs943166 | chrX:69191602 | C>T | SNV | LINC00269 : Intron Variant | AD |
rs5937156 | chrX:69124471 | A>G | SNV | Intergenic | AD |
rs6549184 | chr3:69101126 | G>A | SNV | ARL6IP5 : Intron Variant | AD |
rs2842040 | chr1:69050956 | G>A | SNV | Intergenic | AD |
rs11900784 | chr2:69045364 | A>T | SNV | ANTXR1 : Intron Variant | ND |
rs3925053 | chr12:69038840 | A>G / A>T | SNV | Intergenic | AD |
rs4777102 | chr15:68986207 | C>T | SNV | NOX5 : Intron Variant | AD |
rs2268974 | chr14:68956447 | A>G | SNV | ACTN1 : Intron Variant | AD |
rs4365239 | chr15:68952341 | C>T | SNV | NOX5 : Intron Variant | ND |
rs1195812 | chr12:68947245 | A>G | SNV | CPM : Intron Variant | AD |
rs1144962 | chr12:68941205 | A>G | SNV | CPM : Intron Variant | AD |
rs2300877 | chr14:68939123 | G>T | SNV | ACTN1 : Intron Variant | AD |
rs6770678 | chr3:68911859 | C>T | SNV | FAM19A4 : Intron Variant | AD |
rs8071366 | chr17:68829799 | G>A | SNV | LOC105371874 : Intron Variant | AD |
rs835315 | chr4:68820054 | G>A | SNV | UGT2B10 : Intron Variant | ND |
rs7657958 | chr4:68817077 | G>A | SNV | UGT2B10 : Intron Variant | ND |
rs11228346 | chr11:68774072 | A>G | SNV | CPT1A : Intron Variant | ND |
rs12321570 | chr12:68768463 | T>C | SNV | SLC35E3 : 3 Prime UTR Variant | AD |
rs17674853 | chr17:68755881 | A>G | SNV | Intergenic | AD |
rs8019389 | chr14:68734473 | G>C / G>T | SNV | LOC105370547 : Intron Variant | ND |
rs17279860 | chr15:68726620 | A>T | SNV | CORO2B : 3 Prime UTR Variant | AD |
rs11869735 | chr17:68705649 | A>G | SNV | Intergenic | AD |
rs7032966 | chr9:68596686 | C>T | SNV | LOC105376072 : Intron Variant | AD |
rs2468406 | chr12:68556891 | G>A | SNV | Intergenic | ND |
rs981146 | chr6:68461016 | C>T | SNV | Intergenic | ND |
rs42905 | chr5:68455394 | A>C | SNV | Intergenic | AD |
rs17212908 | chr18:68427994 | C>T | SNV | Intergenic | AD |
rs6501422 | chr17:68393505 | T>C | SNV | ARSG : Intron Variant | AD |
rs17813101 | chr12:68375152 | G>A | SNV | Intergenic | AD |
rs1874243 | chr7:68363094 | G>A / G>C | SNV | Intergenic | AD |
rs1111571 | chr16:68329278 | G>A | SNV | PRMT7 : Intron Variant | AD |
rs1146833 | chr13:68250938 | C>T | SNV | Intergenic | AD |
rs12097456 | chr1:68237404 | C>T | SNV | Intergenic | AD |
rs7650009 | chr3:68203529 | A>G | SNV | FAM19A1 : Intron Variant | AD |
rs683979 | chr18:68186551 | C>T | SNV | Intergenic | ND |
rs9990002 | chr3:68116622 | G>T | SNV | FAM19A1 : Intron Variant | AD |
rs721793 | chr12:68040234 | C>T | SNV | LOC107984526 : Intron Variant | AD |
rs17034763 | chr2:67977281 | C>T | SNV | Intergenic | AD |
rs11870068 | chr17:67948399 | A>C | SNV | BPTF : Intron Variant | AD |
rs8071463 | chr17:67942539 | G>A | SNV | BPTF : Intron Variant | AD |
rs1910370 | chr2:67867965 | G>A | SNV | Intergenic | AD |
rs4607305 | chr5:67714710 | T>C | SNV | Intergenic | AD |
rs2448709 | chr18:67651299 | G>T | SNV | LOC643542 : Intron Variant | AD |
rs4078050 | chr5:67640322 | G>A / G>C / G>T | SNV | LOC105379006 : Intron Variant | AD |
rs7069964 | chr10:67486714 | C>T | SNV | CTNNA3 : Intron Variant | AD |
rs9312182 | chr4:67484590 | T>C / T>G | SNV | CENPC : Intron Variant | AD |
rs1874633 | chr4:67471717 | A>G | SNV | CENPC : Non Coding Transcript Variant | AD |
rs11946612 | chr4:67470253 | T>A / T>C | SNV | CENPC : Non Coding Transcript Variant | AD |
rs10997651 | chr10:67462712 | A>C | SNV | CTNNA3 : Intron Variant | AD |
rs7681618 | chr4:67448722 | A>G | SNV | Intergenic | AD |
rs6810410 | chr4:67443848 | T>C | SNV | Intergenic | AD |
rs17428139 | chr4:67401719 | C>T | SNV | Intergenic | AD |
rs3762317 | chr1:67306899 | A>C / A>G | SNV | IL12RB2 : 2KB Upstream Variant | AD |
rs2394340 | chr10:67101514 | T>C | SNV | LRRTM3 : Non Coding Transcript Variant CTNNA3 : Intron Variant | AD |
rs9351629 | chr6:67093319 | G>A | SNV | Intergenic | AD |
rs6866391 | chr5:67028247 | A>G | SNV | MAST4 : Intron Variant | AD |
rs4235984 | chr6:67028168 | A>G | SNV | Intergenic | AD |
rs4610540 | chr6:66990490 | T>C | SNV | Intergenic | AD |
rs9540953 | chr13:66949126 | T>C | SNV | PCDH9 : Intron Variant | AD |
rs17791001 | chr13:66946882 | A>C | SNV | PCDH9 : Intron Variant | AD |
rs9332406 | chr10:66910441 | C>A | SNV | CTNNA3 : Intron Variant LOC101928961 : Non Coding Transcript Variant | ND |
rs4142041 | chr10:66881193 | A>G | SNV | CTNNA3 : Intron Variant | ND |
rs1880046 | chr10:66878053 | C>T | SNV | CTNNA3 : Intron Variant | ND |
rs422945 | chr16:66832730 | T>G | SNV | NAE1 : 2KB Upstream Variant | AD |
rs11870024 | chr17:66821890 | G>A | SNV | Intergenic | AD |
rs363175 | chr16:66821744 | C>T | SNV | NAE1 : Intron Variant | AD |
rs4791032 | chr17:66820347 | A>G | SNV | Intergenic | AD |
rs10997361 | chr10:66722696 | C>T | SNV | CTNNA3 : Intron Variant | AD |
rs2439353 | chr15:66598146 | C>G / C>T | SNV | LINC01169 : Intron Variant | AD |
rs7159831 | chr14:66562315 | G>A | SNV | GPHN : Intron Variant | AD |
rs484358 | chr11:66551791 | G>A | SNV | ACTN3 : Intron Variant | AD |
rs11079657 | chr17:66435948 | A>G | SNV | PRKCA : Intron Variant | AD |
rs973753 | chr17:66432564 | C>T | SNV | PRKCA : Intron Variant | AD |
rs851860 | chr6:66344991 | A>G | SNV | Intergenic | AD |
rs11863931 | chr16:66344849 | A>G | SNV | Intergenic | AD |
rs1982305 | chr13:66334267 | G>A | SNV | PCDH9 : Intron Variant | AD |
rs8081614 | chr17:66288266 | T>G | SNV | Intergenic | AD |
rs12522102 | chr5:66287270 | A>G | SNV | LOC105379004 : Intron Variant | AD |
rs12728294 | chr1:66274784 | T>C | SNV | PDE4B : Intron Variant | ND |
rs6700403 | chr1:66269918 | T>C | SNV | PDE4B : Intron Variant | ND |
rs10940057 | chr5:66236339 | A>G | SNV | Intergenic | AD |
rs2485381 | chr1:66162049 | G>A | SNV | PDE4B : Intron Variant | AD |
rs12576969 | chr11:66035007 | A>G | SNV | Intergenic | AD |
rs17128103 | chr1:65903182 | C>T | SNV | PDE4B : Intron Variant | AD |
rs4464770 | chr6:65884589 | T>A / T>C | SNV | Intergenic | AD |
rs10940051 | chr5:65811762 | C>T | SNV | NLN : Intron Variant | AD |
rs1670160 | chr10:65785302 | C>T | SNV | LOC105378338 : Intron Variant | AD |
rs4629506 | chr4:65718188 | T>C | SNV | Intergenic | ND |
rs12121677 | chr1:65706287 | T>C | SNV | Intergenic | AD |
rs17241135 | chr5:65653767 | G>A | SNV | TRAPPC13 : Intron Variant | AD |
rs4236943 | chr8:65585325 | G>A | SNV | Intergenic | AD |
rs4941342 | chr18:65527982 | T>C | SNV | Intergenic | AD |
rs11131599 | chr4:65517712 | G>A | SNV | EPHA5 : Intron Variant | AD |
rs1269068 | chr14:65300615 | C>T | SNV | Intergenic | AD |
rs1889925 | chr1:65221873 | G>A / G>T | SNV | AK4 : Intron Variant | AD |
rs1760981 | chr14:65187177 | T>C / T>G | SNV | Intergenic | AD |
rs7141753 | chr14:65179727 | C>T | SNV | Intergenic | AD |
rs1109374 | chr1:65167814 | T>C | SNV | AK4 : Intron Variant | ND |
rs12434868 | chr14:65033431 | G>A | SNV | MAX : Intron Variant CHURC1-FNTB : Intron Variant FNTB : Intron Variant | AD |
rs7148144 | chr14:65032732 | G>A | SNV | MAX : Intron Variant CHURC1-FNTB : Intron Variant FNTB : Intron Variant | AD |
rs7904001 | chr10:65002965 | G>A | SNV | Intergenic | AD |
rs229609 | chr14:64833092 | G>A | SNV | SPTB : Intron Variant | AD |
rs1875053 | chr14:64788300 | C>T | SNV | SPTB : Intron Variant | AD |
rs6911837 | chr6:64787060 | G>A | SNV | EYS : Intron Variant | AD |
rs2899699 | chr15:64620720 | G>T | SNV | ZNF609 : Intron Variant | AD |
rs17300741 | chr11:64563990 | A>G | SNV | SLC22A11 : Intron Variant | AD |
rs1014640 | chr3:64557939 | T>C | SNV | ADAMTS9 : Intron Variant | AD |
rs17126643 | chr1:64544923 | T>G | SNV | CACHD1 : Intron Variant | AD |
rs4688470 | chr3:64511675 | A>C | SNV | Intergenic | AD |
rs16947824 | chr17:64505387 | G>A | SNV | DDX5 : Intron Variant CEP95 : 2KB Upstream Variant | ND |
rs919123 | chr2:64326306 | A>C | SNV | LOC105374768 : Intron Variant | AD |
rs6960379 | chr7:64290139 | T>C | SNV | LOC105375323 : Non Coding Transcript Variant | ND |
rs10995853 | chr10:64259979 | C>G | SNV | LOC105378334 : Intron Variant | OD |
rs12581277 | chr12:64203547 | T>C | SNV | C12orf66 : Intron Variant | AD |
rs2297301 | chr14:64177487 | T>C | SNV | SYNE2 : Intron Variant | ND |
rs1024895 | chr3:64125982 | T>C | SNV | PRICKLE2 : Intron Variant | ND |
rs830010 | chr3:64123061 | C>A | SNV | PRICKLE2 : Intron Variant | ND |
rs3003672 | chr6:64121227 | A>C | SNV | EYS : Intron Variant | AD |
rs1096170 | chr3:64118712 | C>T | SNV | PRICKLE2 : Intron Variant | ND |
rs893779 | chr2:64028052 | T>C | SNV | Intergenic | AD |
rs1530730 | chr4:63978785 | G>A | SNV | Intergenic | AD |
rs13009774 | chr2:63977706 | T>G | SNV | VPS54 : Intron Variant | AD |
rs2275019 | chr14:63941390 | G>C | SNV | SYNE2 : Intron Variant | AD |
rs1345479 | chr2:63903097 | A>G | SNV | VPS54 : Intron Variant | AD |
rs884242 | chr10:63891019 | C>T | SNV | LOC105378332 : Intron Variant | AD |
rs2287361 | chr2:63890506 | C>G / C>T | SNV | UGP2 : Intron Variant | AD |
rs12993544 | chr2:63878419 | A>G | SNV | UGP2 : Intron Variant | AD |
rs12988017 | chr2:63844466 | A>G | SNV | UGP2 : Intron Variant | AD |
rs4427464 | chr10:63828177 | T>G | SNV | Intergenic | AD |
rs10897449 | chr11:63825149 | C>T | SNV | C11orf84 : Intron Variant | AD |
rs6921058 | chr6:63814258 | G>T | SNV | EYS : Intron Variant | AD |
rs756274 | chr6:63795320 | A>G | SNV | EYS : Intron Variant | AD |
rs319920 | chr6:63794359 | A>G | SNV | EYS : Intron Variant | AD |
rs319924 | chr6:63777354 | A>G | SNV | EYS : Intron Variant | AD |
rs620019 | chr1:63775258 | T>C | SNV | ROR1 : Intron Variant | AD |
rs2819130 | chr1:63765870 | G>A | SNV | Intergenic | AD |
rs10042968 | chr5:63737891 | A>G | SNV | Intergenic | ND |
rs13097862 | chr3:63733563 | A>C / A>G / A>T | SNV | Intergenic | OD |
rs12515008 | chr5:63730392 | A>G | SNV | Intergenic | AD |
rs11845765 | chr14:63725032 | T>G | SNV | SGPP1 : Intron Variant | AD |
rs10755432 | chr6:63687952 | A>C | SNV | PHF3 : Intron Variant | AD |
rs7548548 | chr1:63685698 | G>C | SNV | LOC105378771 : Intron Variant | AD |
rs1506397 | chr1:63679612 | C>G | SNV | LOC105378771 : Intron Variant | AD |
rs10485358 | chr6:63676159 | C>T | SNV | PHF3 : Intron Variant | AD |
rs6932538 | chr6:63673079 | C>T | SNV | PHF3 : Intron Variant | AD |
rs2810864 | chr13:63667981 | G>A | SNV | LINC00395 : Intron Variant LOC105370236 : Intron Variant | AD |
rs2749097 | chr1:63661797 | C>G | SNV | Intergenic | AD |
rs855350 | chr1:63661333 | C>T | SNV | Intergenic | AD |
rs4643 | chr1:63659768 | A>C | SNV | PGM1 : 3 Prime UTR Variant | AD |
rs8294 | chr1:63659697 | C>T | SNV | PGM1 : 3 Prime UTR Variant | AD |
rs11208264 | chr1:63659401 | T>C | SNV | PGM1 : Intron Variant | AD |
rs2749100 | chr1:63659308 | G>T | SNV | PGM1 : Intron Variant | AD |
rs1530485 | chr13:63658208 | C>T | SNV | LOC105370236 : Intron Variant | AD |
rs12027168 | chr1:63654942 | T>C | SNV | PGM1 : Intron Variant | AD |
rs2269233 | chr1:63653675 | T>C / T>G | SNV | PGM1 : Intron Variant | AD |
rs2269234 | chr1:63653305 | A>G | SNV | PGM1 : Intron Variant | AD |
rs2269235 | chr1:63653244 | A>G | SNV | PGM1 : Intron Variant | AD |
rs2269238 | chr1:63651866 | G>A / G>T | SNV | PGM1 : Intron Variant | AD |
rs11576729 | chr1:63648758 | G>A / G>T | SNV | PGM1 : Intron Variant | AD |
rs3790857 | chr1:63646195 | C>T | SNV | PGM1 : Intron Variant | AD |
rs2269240 | chr1:63643593 | T>C | SNV | PGM1 : Intron Variant | AD |
rs2269241 | chr1:63643100 | T>C | SNV | PGM1 : Intron Variant | AD |
rs2269245 | chr1:63642222 | G>A | SNV | PGM1 : Intron Variant | AD |
rs2269246 | chr1:63641820 | T>C | SNV | PGM1 : Intron Variant | AD |
rs2269247 | chr1:63641613 | C>T | SNV | PGM1 : Intron Variant | AD |
rs2301054 | chr1:63641357 | A>G | SNV | PGM1 : Intron Variant | AD |
rs7692181 | chr4:63635276 | C>T | SNV | Intergenic | ND |
rs9294269 | chr6:63627392 | A>C | SNV | Intergenic | AD |
rs2911181 | chr16:63563356 | A>G | SNV | LOC105371308 : Intron Variant | AD |
rs11865197 | chr16:63554638 | T>C | SNV | LOC105371308 : Intron Variant | AD |
rs1322416 | chr6:63544114 | T>G | SNV | LGSN : Intron Variant PTP4A1 : Intron Variant | AD |
rs9932227 | chr16:63539610 | C>T | SNV | LOC105371308 : Intron Variant | AD |
rs1197905 | chr6:63525101 | T>C | SNV | LGSN : Intron Variant | AD |
rs1681957 | chr6:63513240 | T>C | SNV | LGSN : Intron Variant | AD |
rs2984458 | chr6:63505258 | T>C | SNV | LGSN : Intron Variant | AD |
rs1744140 | chr6:63502926 | T>C | SNV | LGSN : Intron Variant | AD |
rs2758259 | chr6:63483202 | C>T | SNV | LGSN : Intron Variant | AD |
rs4557499 | chr6:63480642 | G>T | SNV | LGSN : Intron Variant | AD |
rs4299811 | chr6:63480541 | C>T | SNV | LGSN : Intron Variant | AD |
rs9353016 | chr6:63476127 | G>A | SNV | LGSN : Intron Variant | AD |
rs6942342 | chr6:63466542 | T>C | SNV | LGSN : Intron Variant | AD |
rs9449291 | chr6:63453048 | G>A | SNV | LGSN : Intron Variant | AD |
rs7714594 | chr5:63358855 | C>A | SNV | LOC107986418 : Intron Variant | ND |
rs2273500 | chr20:63355597 | T>C | SNV | CHRNA4 : Splice Acceptor Variant | ND |
rs1044396 | chr20:63349782 | G>A / G>C | SNV | CHRNA4 : Missense Variant | ND |
rs2236196 | chr20:63346204 | G>A | SNV | CHRNA4 : Non Coding Transcript Variant | ND |
rs2169520 | chr5:63302626 | T>C | SNV | LOC107986417 : Intron Variant | ND |
rs4700575 | chr5:63300149 | T>A / T>G | SNV | LOC107986417 : Non Coding Transcript Variant | ND |
rs7445832 | chr5:63290474 | T>A | SNV | Intergenic | AD | ND |
rs2459572 | chr6:63283470 | C>T | SNV | LGSN : Intron Variant | OD |
rs349497 | chr5:63258220 | A>C | SNV | Intergenic | AD |
rs6454050 | chr6:63155077 | T>C | SNV | Intergenic | ND |
rs12164904 | chr15:63028335 | C>A / C>G | SNV | Intergenic | AD |
rs2660598 | chr4:62976344 | G>A | SNV | Intergenic | AD |
rs7235367 | chr18:62942490 | G>A | SNV | PHLPP1 : Intron Variant | AD |
rs7556152 | chr1:62918621 | T>G | SNV | Intergenic | AD |
rs7967481 | chr12:62911903 | G>A / G>T | SNV | PPM1H : Intron Variant | AD |
rs10509177 | chr10:62908288 | C>T | SNV | LOC107984012 : Intron Variant | AD |
rs1577822 | chr6:62875235 | T>G | SNV | Intergenic | OD |
rs16945949 | chr15:62853703 | G>A | SNV | Intergenic | AD |
rs1877026 | chr2:62845073 | A>G | SNV | EHBP1 : Intron Variant | ND |
rs12303266 | chr12:62774165 | C>T | SNV | PPM1H : Intron Variant | AD |
rs342171 | chr12:62720730 | T>C | SNV | PPM1H : Intron Variant | AD |
rs12591037 | chr15:62656710 | C>T | SNV | TLN2 : Intron Variant | AD |
rs938979 | chr15:62647241 | T>C | SNV | TLN2 : Intron Variant | AD |
rs17087443 | chr13:62597436 | T>C | SNV | Intergenic | ND |
rs2138564 | chr10:62547558 | C>T | SNV | ZNF365 : Intron Variant | AD |
rs2911292 | chr16:62547042 | C>T | SNV | Intergenic | ND |
rs1997247 | chr2:62530420 | G>A | SNV | TMEM17 : Intron Variant LOC105374764 : Intron Variant | ND |
rs6445276 | chr3:62519585 | T>A / T>C | SNV | CADPS : Intron Variant | ND |
rs6061245 | chr20:62469171 | T>C | SNV | GATA5 : Intron Variant | AD |
rs584274 | chr6:62464512 | C>G | SNV | Intergenic | AD |
rs7523622 | chr1:62424839 | C>A | SNV | LOC105378768 : Intron Variant | AD |
rs75792394 | chr2:62381943 | G>T | SNV | Intergenic | CD |
rs954237 | chr11:62297243 | T>C | SNV | SCGB1D4 : Intron Variant | CD |
rs7605321 | chr2:62204998 | G>A | SNV | B3GNT2 : Intron Variant MIR5192 : 2KB Upstream Variant | AD |
rs6142970 | chr20:62175801 | C>T | SNV | SS18L1 : Intron Variant | AD |
rs6142969 | chr20:62174127 | C>T | SNV | SS18L1 : Intron Variant | AD |
rs10889272 | chr1:61936877 | C>T | SNV | PATJ : Intron Variant | AD |
rs6089556 | chr20:61929031 | T>C | SNV | CDH4 : Intron Variant | ND |
rs6981356 | chr8:61926795 | T>C | SNV | LOC101929628 : Intron Variant | AD |
rs17156580 | chr11:61924869 | C>T | SNV | RAB3IL1 : Intron Variant | AD |
rs4986765 | chr17:61686104 | T>C | SNV | BRIP1 : Synonymous Variant | AD |
rs6551640 | chr4:61653103 | T>A | SNV | ADGRL3 : Intron Variant | ND |
rs26913 | chr5:61634155 | C>T | SNV | Intergenic | AD |
rs2429862 | chr11:61612174 | C>T | SNV | Intergenic | AD |
rs4580548 | chr3:61595375 | C>G / C>T | SNV | PTPRG : Intron Variant | AD |
rs673401 | chr18:61540199 | C>T | SNV | CDH20 : Intron Variant | AD |
rs11079433 | chr17:61507528 | G>A | SNV | Intergenic | AD |
rs2997415 | chr13:61474483 | G>A | SNV | Intergenic | AD |
rs10483734 | chr14:61471083 | T>C | SNV | PRKCH : Intron Variant | AD |
rs778139 | chr2:61457429 | G>A | SNV | USP34 : Intron Variant | AD |
rs767755 | chr14:61407730 | G>A | SNV | PRKCH : Intron Variant | AD |
rs12607636 | chr18:61341069 | G>A | SNV | CDH20 : Intron Variant | ND |
rs12101174 | chr14:61332107 | A>G | SNV | PRKCH : Intron Variant | ND |
rs868827 | chr14:61235011 | G>A | SNV | Intergenic | AD |
rs11071587 | chr15:61141344 | G>A | SNV | RORA : Intron Variant | AD |
rs6445194 | chr3:61125522 | G>T | SNV | FHIT : Intron Variant | AD |
rs9825823 | chr3:61096480 | T>C | SNV | FHIT : Intron Variant | AD |
rs13279512 | chr8:61045943 | G>A | SNV | Intergenic | OD |
rs1909766 | chr16:61027486 | T>C | SNV | Intergenic | AD |
rs6071447 | chr20:60949614 | C>T | SNV | Intergenic | AD |
rs17064083 | chr3:60866766 | C>G | SNV | FHIT : Intron Variant | AD |
rs3763591 | chr8:60851830 | G>T | SNV | CHD7 : Intron Variant | AD |
rs10153975 | chr20:60815936 | T>C | SNV | Intergenic | AD |
rs2456769 | chr10:60799084 | T>A / T>C | SNV | Intergenic | CD |
rs2456778 | chr10:60792132 | A>T | SNV | CDK1 : Intron Variant | CD |
rs2448363 | chr10:60790961 | C>T | SNV | CDK1 : Intron Variant | CD |
rs744383 | chr10:60777020 | T>C | SNV | CDK1 : 2KB Upstream Variant | CD |
rs11993480 | chr8:60744514 | A>G / A>T | SNV | CHD7 : Intron Variant | ND |
rs1904397 | chr10:60734102 | C>A | SNV | ANK3 : 2KB Upstream Variant LOC105378320 : Intron Variant | CD |
rs1735460 | chr3:60705872 | T>C | SNV | FHIT : Intron Variant | AD |
rs1735457 | chr3:60698004 | G>A | SNV | FHIT : Intron Variant | AD |
rs12865240 | chr13:60545223 | A>G | SNV | TDRD3 : Intron Variant | AD |
rs9538740 | chr13:60535829 | A>G | SNV | TDRD3 : Intron Variant | AD |
rs9538710 | chr13:60461664 | G>A | SNV | TDRD3 : Intron Variant | AD |
rs4886227 | chr13:60416372 | A>G | SNV | TDRD3 : Intron Variant | AD |
rs8050990 | chr16:60361443 | C>T | SNV | LOC101927605 : Intron Variant LOC729159 : 2KB Upstream Variant | AD |
rs10821716 | chr10:60310995 | C>T | SNV | ANK3 : Intron Variant | AD |
rs77993859 | chr15:60155639 | G>C | SNV | Intergenic | AD |
rs17062350 | chr3:60143118 | C>T | SNV | FHIT : Intron Variant | AD |
rs10821687 | chr10:60142442 | C>T | SNV | ANK3 : Intron Variant | ND |
rs7411728 | chr1:59981117 | G>A | SNV | Intergenic | AD |
rs931317 | chr3:59943125 | A>G | SNV | FHIT : Intron Variant | ND |
rs6479671 | chr10:59938119 | G>A | SNV | Intergenic | AD |
rs7595950 | chr2:59916057 | T>C | SNV | Intergenic | AD |
rs6070956 | chr20:59809755 | C>G / C>T | SNV | PHACTR3 : Intron Variant | AD |
rs6027132 | chr20:59809396 | C>T | SNV | PHACTR3 : Intron Variant | AD |
rs11125811 | chr2:59760639 | T>C | SNV | Intergenic | AD |
rs17050411 | chr2:59752369 | T>C | SNV | Intergenic | AD |
rs10851664 | chr15:59708040 | G>C | SNV | Intergenic | AD |
rs12438078 | chr15:59696273 | G>C | SNV | Intergenic | AD |
rs2852356 | chr18:59692901 | G>A | SNV | CCBE1 : Intron Variant | ND |
rs1944980 | chr18:59616901 | C>T | SNV | CCBE1 : Intron Variant | AD |
rs721250 | chr2:59549881 | C>A / C>T | SNV | Intergenic | AD |
rs2215906 | chr2:59548430 | C>A / C>T | SNV | Intergenic | AD |
rs887942 | chr2:59548033 | G>C | SNV | Intergenic | AD |
rs2418867 | chr2:59545467 | C>T | SNV | Intergenic | AD |
rs10195005 | chr2:59544505 | G>A | SNV | Intergenic | AD |
rs2674079 | chr2:59544344 | A>C / A>T | SNV | Intergenic | AD |
rs2674052 | chr2:59543218 | T>A / T>G | SNV | Intergenic | AD |
rs2674050 | chr2:59542182 | C>T | SNV | Intergenic | AD |
rs7571858 | chr2:59542138 | G>A / G>T | SNV | Intergenic | AD |
rs2540083 | chr2:59542015 | G>A | SNV | Intergenic | AD |
rs2674048 | chr2:59541877 | C>G / C>T | SNV | Intergenic | AD |
rs2674047 | chr2:59541550 | T>A | SNV | Intergenic | AD |
rs2674046 | chr2:59541006 | C>T | SNV | Intergenic | AD |
rs2674067 | chr2:59538549 | A>G | SNV | Intergenic | AD |
rs2540087 | chr2:59535459 | C>A | SNV | Intergenic | AD |
rs2540088 | chr2:59535425 | C>A / C>G | SNV | Intergenic | AD |
rs2540089 | chr2:59535236 | C>T | SNV | Intergenic | AD |
rs2674041 | chr2:59530366 | G>A | SNV | Intergenic | AD |
rs2540096 | chr2:59529719 | T>A / T>C | SNV | Intergenic | AD |
rs2540097 | chr2:59528529 | A>G | SNV | Intergenic | AD |
rs56093216 | chr2:59526837 | T>C | SNV | Intergenic | AD |
rs2540098 | chr2:59526674 | C>T | SNV | Intergenic | AD |
rs2540099 | chr2:59526606 | C>T | SNV | Intergenic | AD |
rs2674061 | chr2:59526196 | C>T | SNV | Intergenic | AD |
rs7164726 | chr15:59423467 | C>T | SNV | FAM81A : Intron Variant | AD |
rs10519005 | chr15:59419492 | C>T | SNV | FAM81A : Intron Variant | AD |
rs17644588 | chr2:59353191 | G>A | SNV | LOC105374754 : Intron Variant | ND |
rs181048070 | chr2:59316241 | G>A | SNV | LOC105374754 : Intron Variant | AD |
rs7835993 | chr8:59308573 | G>A | SNV | Intergenic | AD |
rs6997052 | chr8:59301470 | G>A | SNV | Intergenic | AD |
rs17780175 | chr5:59293960 | G>A | SNV | PDE4D : Intron Variant | ND |
rs12142820 | chr1:59250371 | A>T | SNV | Intergenic | AD |
rs7991723 | chr13:59153386 | C>G / C>T | SNV | Intergenic | AD |
rs2137457 | chr3:59120187 | G>A | SNV | LOC105377110 : Intron Variant | AD |
rs4940444 | chr18:59085268 | T>C | SNV | Intergenic | AD |
rs422729 | chr8:58995470 | A>G | SNV | TOX : Intron Variant | ND |
rs11807036 | chr1:58982247 | A>G | SNV | LOC105378753 : Intron Variant | AD |
rs7245090 | chr18:58968091 | T>G | SNV | ZNF532 : Intron Variant | AD |
rs4074334 | chr4:58939738 | T>G | SNV | Intergenic | AD |
rs550864 | chr11:58926213 | G>T | SNV | GLYATL1 : 2KB Upstream Variant | AD |
rs17761525 | chr18:58911721 | C>T | SNV | ZNF532 : Intron Variant | AD |
rs17118349 | chr1:58885471 | C>T | SNV | LINC01135 : Intron Variant LOC105378753 : Intron Variant | AD |
rs28570064 | chr4:58868046 | A>G | SNV | Intergenic | AD |
rs7685041 | chr4:58854266 | G>A | SNV | Intergenic | AD |
rs17552189 | chr2:58845834 | C>T | SNV | LINC01122 : Intron Variant | AD |
rs442555 | chr14:58829466 | T>C | SNV | LINC01500 : Intron Variant | AD |
rs7333252 | chr13:58774130 | T>C | SNV | Intergenic | AD |
rs2319974 | chr18:58749237 | A>G | SNV | MALT1 : Non Coding Transcript Variant | ND |
rs1014968 | chr11:58673247 | C>T | SNV | Intergenic | AD |
rs12798524 | chr11:58671182 | A>G | SNV | Intergenic | AD |
rs7101281 | chr10:58661978 | T>A | SNV | BICC1 : Intron Variant | ND |
rs116087723 | chr17:58507645 | C>T | SNV | MTMR4 : Intron Variant | CD |
rs6895889 | chr5:58490716 | G>T | SNV | GAPT : 2KB Upstream Variant | AD |
rs6865094 | chr5:58487236 | C>T | SNV | Intergenic | AD |
rs114903983 | chr17:58483499 | T>C | SNV | HSF5 : Intron Variant | CD |
rs7240666 | chr18:58481867 | T>C | SNV | ALPK2 : Missense Variant | AD |
rs114469297 | chr17:58411019 | A>C / A>G | SNV | RNF43 : Intron Variant | CD |
rs113212925 | chr17:58373093 | C>G / C>T | SNV | RNF43 : Intron Variant | CD |
rs7199896 | chr16:58339080 | T>A | SNV | Intergenic | AD |
rs11885675 | chr2:58295526 | T>A | SNV | LOC105374744 : Intron Variant | AD |
rs4681824 | chr3:58213942 | T>G | SNV | LOC107986091 : Non Coding Transcript Variant | AD |
rs12261547 | chr10:58209350 | G>C | SNV | IPMK : Intron Variant | AD |
rs11854297 | chr15:58182926 | T>C | SNV | AQP9 : Intron Variant LOC101928635 : Intron Variant | AD |
rs1622626 | chr10:58172751 | A>C | SNV | Intergenic | ND |
rs1622669 | chr10:58172737 | A>G | SNV | Intergenic | ND |
rs4681795 | chr3:58150702 | T>C | SNV | FLNB : Intron Variant | AD |
rs6128273 | chr20:58144617 | C>A | SNV | LOC107985434 : Intron Variant | AD |
rs1006438 | chr16:58138699 | T>C / T>G | SNV | LOC101927556 : Non Coding Transcript Variant | AD |
rs2362904 | chr3:58126761 | C>T | SNV | FLNB : Synonymous Variant | AD |
rs4681800 | chr3:58124021 | T>A | SNV | FLNB : Intron Variant | AD |
rs7615893 | chr3:58112717 | T>C | SNV | FLNB : Intron Variant | AD |
rs11648508 | chr16:58029609 | G>T | SNV | MMP15 : Intron Variant | AD |
rs12435601 | chr14:57979379 | G>T | SNV | SLC35F4 : Intron Variant | AD |
rs17625382 | chr10:57812948 | G>A | SNV | LOC105378314 : Intron Variant | AD |
rs7909889 | chr10:57812610 | C>T | SNV | LOC105378314 : Intron Variant | AD |
rs11594537 | chr10:57800925 | T>C | SNV | LOC105378314 : Intron Variant | AD |
rs56299213 | chr10:57799559 | C>T | SNV | LOC105378314 : Intron Variant | AD |
rs17625002 | chr10:57799360 | T>G | SNV | LOC105378314 : Intron Variant | AD |
rs7544843 | chr1:57798095 | G>A | SNV | DAB1 : Intron Variant | AD |
rs7554147 | chr1:57791915 | T>C | SNV | DAB1 : Intron Variant | AD |
rs1323838 | chr1:57791578 | T>C | SNV | DAB1 : Intron Variant | AD |
rs35738462 | chr1:57790872 | T>A / T>C | SNV | DAB1 : Intron Variant | AD |
rs12568292 | chr1:57790519 | C>A | SNV | DAB1 : Intron Variant | AD |
rs12565523 | chr1:57790476 | T>G | SNV | DAB1 : Intron Variant | AD |
rs10877015 | chr12:57774005 | A>G | SNV | METTL21B : Intron Variant METTL1 : 2KB Upstream Variant | AD |
rs10096565 | chr8:57757793 | A>C / A>T | SNV | Intergenic | AD |
rs9694511 | chr8:57751729 | T>C | SNV | Intergenic | AD |
rs7004631 | chr8:57704061 | G>A | SNV | Intergenic | AD |
rs1425948 | chr15:57665116 | A>G | SNV | GCOM1 : Intron Variant MYZAP : Intron Variant | AD |
rs11071339 | chr15:57663371 | C>A | SNV | GCOM1 : Intron Variant MYZAP : Intron Variant | AD |
rs2433196 | chr15:57643221 | A>C | SNV | GCOM1 : Intron Variant MYZAP : Intron Variant | AD |
rs7176042 | chr15:57642503 | G>A / G>T | SNV | GCOM1 : Intron Variant MYZAP : Intron Variant | AD |
rs6099690 | chr20:57635380 | T>C | SNV | Intergenic | ND |
rs4811895 | chr20:57631253 | G>A | SNV | Intergenic | ND |
rs718307 | chr20:57630973 | G>A | SNV | Intergenic | ND |
rs17239999 | chr15:57626376 | C>T | SNV | GCOM1 : Intron Variant MYZAP : Intron Variant | AD |
rs9920308 | chr15:57610033 | C>A | SNV | GCOM1 : Intron Variant MYZAP : Intron Variant | CD |
rs2325777 | chr8:57601527 | C>T | SNV | Intergenic | AD |
rs744318 | chr15:57589691 | T>A / T>G | SNV | Intergenic | AD |
rs11071334 | chr15:57586613 | T>C | SNV | Intergenic | AD |
rs935549 | chr15:57581240 | C>T | SNV | Intergenic | AD |
rs11623923 | chr14:57576035 | G>A | SNV | SLC35F4 : Intron Variant LOC105370519 : Intron Variant | AD |
rs7179379 | chr15:57567529 | C>T | SNV | Intergenic | AD |
rs2600003 | chr12:57559461 | A>C / A>T | SNV | KIF5A : Intron Variant | AD |
rs6581146 | chr12:57552694 | C>T | SNV | KIF5A : Intron Variant | AD |
rs1148551 | chr12:57552077 | G>A | SNV | KIF5A : Intron Variant | AD |
rs1148552 | chr12:57549189 | C>T | SNV | DCTN2 : 2KB Upstream Variant KIF5A : 2KB Upstream Variant | AD |
rs703841 | chr12:57548522 | T>G | SNV | DCTN2 : 2KB Upstream Variant KIF5A : 2KB Upstream Variant | AD |
rs17796038 | chr14:57547477 | G>A / G>T | SNV | LOC105370519 : Intron Variant | AD |
rs775238 | chr12:57544298 | C>T | SNV | DCTN2 : Intron Variant | AD |
rs11840092 | chr13:57540614 | T>C | SNV | Intergenic | AD |
rs17795775 | chr14:57532149 | C>T | SNV | LOC105370519 : Intron Variant | AD |
rs1148556 | chr12:57523742 | C>T | SNV | MBD6 : Intron Variant | AD |
rs7997918 | chr13:57516077 | A>C | SNV | LOC105370217 : Intron Variant | AD |
rs61116530 | chr13:57511431 | T>C | SNV | LOC105370217 : Intron Variant | AD |
rs2346471 | chr14:57496259 | A>G | SNV | LOC105370519 : Intron Variant | AD |
rs59972978 | chr20:57483299 | A>T | SNV | Intergenic | AD |
rs11840139 | chr13:57480807 | T>C | SNV | LOC105370217 : Intron Variant | AD |
rs11841410 | chr13:57480649 | A>C | SNV | LOC105370217 : Intron Variant | AD |
rs2220846 | chr5:57479107 | T>C | SNV | Intergenic | AD |
rs7984728 | chr13:57475100 | C>G / C>T | SNV | LOC105370217 : Intron Variant | AD |
rs57558300 | chr13:57466458 | A>G | SNV | LOC105370217 : Intron Variant | AD |
rs7337578 | chr13:57459756 | C>T | SNV | LOC105370217 : Intron Variant | AD |
rs7338789 | chr13:57459659 | T>A / T>C | SNV | LOC105370217 : Intron Variant | AD |
rs6561934 | chr13:57459417 | C>T | SNV | LOC105370217 : Intron Variant | AD |
rs8034838 | chr15:57441989 | G>C | SNV | CGNL1 : Intron Variant | AD |
rs7144713 | chr14:57433176 | T>C | SNV | Intergenic | AD |
rs12440459 | chr15:57402740 | C>T | SNV | CGNL1 : Intron Variant | AD |
rs7144649 | chr14:57355498 | G>A | SNV | Intergenic | AD |
rs9890811 | chr17:57335100 | A>G | SNV | MSI2 : Intron Variant | ND |
rs4774925 | chr15:57312204 | T>C | SNV | Intergenic | ND |
rs3746228 | chr19:57292994 | G>A | SNV | ZNF460 : 3 Prime UTR Variant | AD |
rs10498486 | chr14:57292674 | T>C | SNV | AP5M1 : 3 Prime UTR Variant | AD |
rs2097983 | chr19:57269727 | A>C | SNV | LOC105372476 : Intron Variant | AD |
rs17093036 | chr14:57267302 | C>G | SNV | EXOC5 : Intron Variant AP5M1 : 2KB Upstream Variant | AD |
rs6573140 | chr14:57266276 | T>G | SNV | EXOC5 : Intron Variant | AD |
rs10147752 | chr14:57265552 | A>G | SNV | EXOC5 : Intron Variant | AD |
rs11850616 | chr14:57265255 | C>T | SNV | EXOC5 : Intron Variant | AD |
rs10141911 | chr14:57264133 | C>T | SNV | EXOC5 : Intron Variant | AD |
rs10141811 | chr14:57264030 | C>T | SNV | EXOC5 : Intron Variant | AD |
rs716690 | chr14:57261934 | C>A / C>T | SNV | EXOC5 : Intron Variant | AD |
rs10133300 | chr14:57256175 | G>T | SNV | EXOC5 : Intron Variant | AD |
rs7147218 | chr14:57255339 | T>C / T>G | SNV | EXOC5 : Intron Variant | AD |
rs10130359 | chr14:57249675 | C>T | SNV | EXOC5 : Intron Variant | AD |
rs9323304 | chr14:57245764 | A>C / A>T | SNV | EXOC5 : Intron Variant | AD |
rs6573137 | chr14:57233186 | A>G / A>T | SNV | EXOC5 : Intron Variant | AD |
rs12130571 | chr1:57232328 | C>A | SNV | DAB1 : Intron Variant | AD |
rs7155721 | chr14:57230712 | A>C | SNV | EXOC5 : Intron Variant | AD |
rs10147790 | chr14:57226318 | T>A | SNV | EXOC5 : Intron Variant | AD |
rs11846972 | chr14:57222138 | A>T | SNV | EXOC5 : Intron Variant | AD |
rs1555788 | chr14:57218454 | A>C | SNV | EXOC5 : Intron Variant | AD |
rs60328452 | chr14:57217583 | A>T | SNV | EXOC5 : Intron Variant | AD |
rs10135879 | chr14:57217416 | T>C | SNV | EXOC5 : Intron Variant | AD |
rs4569162 | chr14:57215062 | T>C | SNV | EXOC5 : Intron Variant | AD |
rs10140993 | chr14:57212739 | C>T | SNV | EXOC5 : Intron Variant | AD |
rs10150771 | chr14:57208467 | C>G / C>T | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs10137379 | chr14:57208149 | T>C | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs7141911 | chr14:57206153 | A>G / A>T | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs3742578 | chr14:57205997 | C>T | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs3742577 | chr14:57205822 | T>C | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs8003535 | chr14:57205286 | G>A / G>T | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs7157608 | chr14:57204497 | T>C | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs4612984 | chr14:57204241 | T>C | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs10134311 | chr14:57203324 | C>T | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs11851015 | chr14:57202815 | A>G | SNV | EXOC5 : 3 Prime UTR Variant | AD |
rs10137456 | chr14:57202285 | T>C | SNV | EXOC5 : 500B Downstream Variant | AD |
rs10135064 | chr14:57202141 | T>C / T>G | SNV | EXOC5 : 500B Downstream Variant | AD |
rs10145188 | chr14:57201278 | G>T | SNV | Intergenic | AD |
rs2881345 | chr14:57201005 | C>A / C>T | SNV | Intergenic | AD |
rs17115341 | chr1:57200259 | C>G / C>T | SNV | DAB1 : Intron Variant | AD |
rs10136042 | chr14:57199043 | C>A / C>T | SNV | Intergenic | AD |
rs10135962 | chr14:57198989 | C>G | SNV | Intergenic | AD |
rs2078519 | chr14:57198781 | A>G | SNV | Intergenic | AD |
rs1961293 | chr14:57198361 | G>A | SNV | Intergenic | AD |
rs6573135 | chr14:57197656 | G>C | SNV | Intergenic | AD |
rs767505 | chr16:57178738 | A>G | SNV | FAM192A : Intron Variant | AD |
rs11639875 | chr16:57079952 | C>T | SNV | NLRC5 : Intron Variant | AD |
rs35769988 | chr4:57050723-57050738 | delT | Indel | IGFBP7 : Intron Variant | AD |
rs8108432 | chr19:57023884 | A>G | SNV | Intergenic | AD |
rs36065736 | chr8:56985796 | G>A | SNV | IMPAD1 : Intron Variant | AD |
rs856843 | chr1:56961578 | C>A / C>T | SNV | C8B : Intron Variant | AD |
rs605648 | chr1:56929578 | T>C / T>G | SNV | C8B : Intron Variant | AD |
rs2525994 | chr17:56899561 | C>A | SNV | TRIM25 : Intron Variant | AD |
rs11916112 | chr3:56890683 | G>A | SNV | ARHGEF3 : Intron Variant | AD |
rs2229882 | chr5:56872885 | C>T | SNV | MAP3K1 : Synonymous Variant | AD |
rs17750015 | chr18:56730391 | T>C | SNV | WDR7 : Intron Variant | AD |
rs16886113 | chr5:56699208 | T>G | SNV | Intergenic | AD |
rs2108831 | chr17:56640543 | G>C / G>T | SNV | Intergenic | CD |
rs1907926 | chr10:56579481 | T>A / T>C | SNV | Intergenic | ND |
rs1909749 | chr16:56578790 | C>T | SNV | Intergenic | AD |
rs11623335 | chr14:56566358 | G>A | SNV | Intergenic | AD |
rs13406625 | chr2:56494872 | T>C | SNV | Intergenic | AD |
rs17047975 | chr2:56461262 | A>G | SNV | Intergenic | AD |
rs6421495 | chr1:56439773 | T>A | SNV | Intergenic | AD |
rs5913935 | chrX:56401840 | C>T | SNV | Intergenic | AD |
rs11902680 | chr2:56384590 | C>A | SNV | CCDC85A : 3 Prime UTR Variant | AD |
rs17047868 | chr2:56382236 | G>A | SNV | CCDC85A : Intron Variant | AD |
rs2193488 | chr2:56381681 | G>A / G>T | SNV | CCDC85A : Intron Variant | AD |
rs17047859 | chr2:56373534 | A>C | SNV | CCDC85A : Intron Variant | AD |
rs9808416 | chr2:56336687 | C>T | SNV | CCDC85A : Intron Variant | AD |
rs27006 | chr5:56271754 | G>A | SNV | Intergenic | AD |
rs1357741 | chr7:56223477 | G>A | SNV | Intergenic | AD |
rs10248609 | chr7:56194361 | C>T | SNV | Intergenic | AD |
rs6014619 | chr20:56171081 | C>G | SNV | LOC105372680 : 2KB Upstream Variant | AD |
rs1352010 | chr3:56152208 | A>G | SNV | ERC2 : Intron Variant | AD |
rs16986899 | chr19:56038144 | T>C | SNV | NLRP5 : Missense Variant | ND |
rs1347093 | chr2:56019205 | G>T | SNV | MIR217HG : Intron Variant LOC105374690 : Intron Variant | AD |
rs4553860 | chr2:56016961 | A>G | SNV | MIR217HG : Intron Variant LOC105374690 : Intron Variant | AD |
rs4801658 | chr19:56004228 | T>C | SNV | NLRP5 : Intron Variant | ND |
rs13029542 | chr2:56001216 | C>T | SNV | MIR217HG : Intron Variant MIR216B : 2KB Upstream Variant LOC105374690 : Intron Variant | AD |
rs1370271 | chr20:55965963 | T>C | SNV | Intergenic | AD |
rs6417935 | chrX:55934291 | T>C | SNV | KLF8 : Intron Variant | AD |
rs17288603 | chr3:55921186 | G>A | SNV | ERC2 : Intron Variant | AD |
rs2033316 | chr2:55913396 | A>G | SNV | EFEMP1 : Intron Variant | AD |
rs7631846 | chr3:55849368 | T>C | SNV | ERC2 : Intron Variant | AD |
rs6782906 | chr3:55847492 | C>A / C>T | SNV | ERC2 : Intron Variant | AD |
rs1423071 | chr19:55782335 | G>A | SNV | Intergenic | AD |
rs2414433 | chr15:55751991 | T>C | SNV | Intergenic | AD |
rs7707639 | chr5:55715135 | G>A | SNV | Intergenic | AD |
rs9656709 | chr7:55656752 | A>C | SNV | Intergenic | AD |
rs9597202 | chr13:55535037 | A>G | SNV | Intergenic | AD |
rs9597180 | chr13:55445756 | A>G | SNV | Intergenic | AD |
rs4630612 | chr17:55420404 | A>G | SNV | MMD : Intron Variant | AD |
rs12518892 | chr5:55404055 | A>G | SNV | SKIV2L2 : Intron Variant | ND |
rs2979062 | chr8:55402359 | T>C | SNV | XKR4 : Intron Variant | ND |
rs888206 | chr17:55390852 | C>T | SNV | Intergenic | AD |
rs17128434 | chr14:55386810 | G>A | SNV | ATG14 : Intron Variant | ND |
rs9597162 | chr13:55347724 | G>A | SNV | Intergenic | AD |
rs678892 | chr15:55340661 | G>A / G>C / G>T | SNV | PIGB : Stop Gained | CD |
rs11084394 | chr19:55330677 | T>C | SNV | TMEM150B : Intron Variant | AD |
rs10876740 | chr12:55322580 | A>G | SNV | Intergenic | AD |
rs13154710 | chr5:55315905 | A>G | SNV | SKIV2L2 : Intron Variant | ND |
rs9316778 | chr13:55287020 | T>C | SNV | Intergenic | AD |
rs9537050 | chr13:55278916 | A>G / A>T | SNV | Intergenic | AD |
rs1437396 | chr2:55278320 | C>T | SNV | Intergenic | AD |
rs459737 | chr3:55271856 | A>G | SNV | Intergenic | AD |
rs11071175 | chr15:55268227 | A>G | SNV | RAB27A : Intron Variant | AD |
rs4261468 | chr15:55263404 | A>G | SNV | RAB27A : Intron Variant | AD |
rs897669 | chr5:55263144 | G>A | SNV | DHX29 : Intron Variant | ND |
rs4146540 | chr13:55262595 | A>G | SNV | Intergenic | AD |
rs4473307 | chr19:55255438 | T>G | SNV | PPP6R1 : Intron Variant | AD |
rs12523234 | chr5:55254871 | A>G | SNV | Intergenic | ND |
rs12857116 | chr13:55220980 | T>G | SNV | Intergenic | AD |
rs2247977 | chr10:55213052 | G>A | SNV | PCDH15 : Intron Variant | AD |
rs12109297 | chr5:55192996 | G>A | SNV | Intergenic | ND |
rs10825471 | chr10:55140878 | A>G | SNV | PCDH15 : Intron Variant | AD |
rs10417874 | chr19:55121025 | G>A | SNV | Intergenic | AD |
rs2305949 | chr4:55114289 | C>A / C>T | SNV | KDR : Intron Variant | AD |
rs2877260 | chr7:55103936 | A>G | SNV | EGFR : Intron Variant | AD |
rs13333707 | chr16:55084886 | C>T | SNV | Intergenic | AD |
rs1613662 | chr19:55025227 | G>A | SNV | GP6 : Missense Variant LOC107985325 : Intron Variant | CD |
rs2304167 | chr19:55015713 | C>T | SNV | GP6 : Missense Variant LOC107985325 : Intron Variant | CD |
rs1654413 | chr19:55014991 | A>T | SNV | GP6 : Missense Variant LOC107985325 : Intron Variant | CD |
rs1671152 | chr19:55014977 | T>G | SNV | GP6 : Missense Variant LOC107985325 : Intron Variant | CD |
rs1671151 | chr19:55014526 | G>A | SNV | GP6 : Synonymous Variant LOC107985325 : Intron Variant | CD |
rs1671150 | chr19:55014129 | A>G | SNV | GP6 : Missense Variant LOC107985325 : Intron Variant | CD |
rs3773586 | chr3:54974719 | C>A | SNV | CACNA2D3 : Intron Variant | ND |
rs2252795 | chr12:54949844 | A>G | SNV | TESPA1 : Non Coding Transcript Variant | AD |
rs7522847 | chr1:54929005 | A>G | SNV | LOC107984959 : Intron Variant | CD |
rs283277 | chr20:54920285 | C>A | SNV | Intergenic | ND |
rs2163618 | chr2:54884552 | G>A | SNV | EML6 : Intron Variant | AD |
rs75104126 | chr13:54883367 | C>A / C>T | SNV | Intergenic | AD |
rs13385982 | chr2:54876128 | G>T | SNV | EML6 : Intron Variant | AD |
rs3826878 | chr19:54865756 | A>G / A>T | SNV | KIR3DL2 : Intron Variant | AD |
rs6810058 | chr3:54857572 | G>T | SNV | CACNA2D3 : Intron Variant | AD |
rs17084794 | chr4:54753866 | C>A | SNV | Intergenic | AD |
rs11845379 | chr14:54727746 | T>C | SNV | SAMD4A : Intron Variant | AD |
rs2414358 | chr15:54682301 | T>A | SNV | Intergenic | AD |
rs1471450 | chr13:54670721 | G>A | SNV | Intergenic | AD |
rs911620 | chr14:54658981 | T>C | SNV | SAMD4A : Intron Variant | ND |
rs475048 | chr7:54641780 | T>A | SNV | Intergenic | AD |
rs1368882 | chr1:54641346 | G>A | SNV | MROH7 : 2KB Upstream Variant MROH7-TTC4 : 2KB Upstream Variant | AD | ND |
rs17563093 | chr7:54640363 | A>G | SNV | Intergenic | AD |
rs56247223 | chr3:54608201 | G>A | SNV | CACNA2D3 : Intron Variant | ND |
rs12980993 | chr19:54593944 | A>C | SNV | LILRA1 : Intron Variant | AD |
rs10402506 | chr19:54563023 | A>G | SNV | LOC107985347 : Intron Variant LOC105372461 : Intron Variant | AD |
rs16953659 | chr16:54553520 | A>G | SNV | LOC105371273 : Intron Variant | ND |
rs7731258 | chr5:54415292 | G>A | SNV | LINC01033 : 500B Downstream Variant | AD |
rs2019089 | chr17:54360132 | A>G | SNV | Intergenic | AD |
rs952766 | chr13:54341371 | G>A | SNV | Intergenic | AD |
rs11708620 | chr3:54337764 | C>T | SNV | CACNA2D3 : Intron Variant | AD |
rs1935468 | chr10:54323965 | T>C | SNV | PCDH15 : Intron Variant | ND |
rs7431992 | chr3:54319213 | T>A | SNV | CACNA2D3 : Intron Variant | ND |
rs4430687 | chr15:54310022 | C>G | SNV | UNC13C : Intron Variant | ND |
rs35951 | chr5:54296531 | G>T | SNV | ARL15 : Intron Variant | AD |
rs35952 | chr5:54296333 | C>T | SNV | ARL15 : Intron Variant | AD |
rs7704911 | chr5:54291872 | C>T | SNV | ARL15 : Intron Variant | AD |
rs4927081 | chr1:54290669 | T>C | SNV | SSBP3 : Intron Variant | AD |
rs6450184 | chr5:54286675 | G>C | SNV | ARL15 : Intron Variant | AD |
rs7725454 | chr5:54286570 | A>T | SNV | ARL15 : Intron Variant | AD |
rs3776641 | chr5:54286422 | C>T | SNV | ARL15 : Intron Variant | AD |
rs3776642 | chr5:54286396 | T>G | SNV | ARL15 : Intron Variant | AD |
rs10940373 | chr5:54279861 | A>G | SNV | ARL15 : Intron Variant | AD |
rs41151 | chr5:54269224 | G>A / G>C / G>T | SNV | ARL15 : Intron Variant | AD |
rs388337 | chr5:54261708 | C>T | SNV | ARL15 : Intron Variant | AD |
rs3857282 | chr5:54248075 | G>C | SNV | ARL15 : Intron Variant | AD |
rs6872430 | chr5:54245925 | G>A | SNV | ARL15 : Intron Variant | AD |
rs6872062 | chr5:54245723 | G>A | SNV | ARL15 : Intron Variant | AD |
rs166093 | chr5:54245095 | G>A | SNV | ARL15 : Intron Variant | AD |
rs3797237 | chr5:54241912 | G>A | SNV | ARL15 : Intron Variant | AD |
rs250378 | chr5:54241769 | G>T | SNV | ARL15 : Intron Variant | AD |
rs2407405 | chr5:54241716 | C>T | SNV | ARL15 : Intron Variant | AD |
rs10044346 | chr5:54241324 | C>T | SNV | ARL15 : Intron Variant | AD |
rs9292042 | chr5:54241168 | C>T | SNV | ARL15 : Intron Variant | AD |
rs12233919 | chr5:54239714 | A>G | SNV | ARL15 : Intron Variant | AD |
rs3910951 | chr5:54239417 | C>T | SNV | ARL15 : Intron Variant | AD |
rs33282 | chr5:54235475 | C>T | SNV | ARL15 : Intron Variant | AD |
rs8060235 | chr16:54231853 | G>A | SNV | Intergenic | AD |
rs8036265 | chr15:54183938 | G>A | SNV | UNC13C : Intron Variant | AD |
rs16953047 | chr16:54096258 | G>T | SNV | FTO : Intron Variant | AD |
rs9303345 | chr17:54079183 | T>A | SNV | Intergenic | AD |
rs750379 | chr3:54077850 | T>C | SNV | Intergenic | AD |
rs11170792 | chr12:54057092 | G>A | SNV | FLJ12825 : 2KB Upstream Variant | AD |
rs16952906 | chr16:54049255 | T>C | SNV | FTO : Intron Variant | ND |
rs2302673 | chr16:54034209 | T>C | SNV | FTO : Intron Variant | ND |
rs13331869 | chr16:54032082 | T>A | SNV | FTO : Intron Variant | ND |
rs6956800 | chr7:53966977 | T>C | SNV | Intergenic | AD |
rs10735853 | chr12:53924362 | T>C | SNV | Intergenic | AD |
rs1362571 | chr16:53877858 | G>A / G>T | SNV | FTO : Intron Variant | AD |
rs2102010 | chr4:53877079 | A>G | SNV | Intergenic | ND |
rs10521308 | chr16:53831214 | G>A | SNV | FTO : Intron Variant | ND |
rs8091046 | chr18:53771958 | A>G | SNV | Intergenic | AD |
rs12251255 | chr10:53760519 | T>G | SNV | Intergenic | AD |
rs12075528 | chr1:53733811 | C>T | SNV | GLIS1 : Intron Variant | AD |
rs797913 | chr1:53732889 | C>T | SNV | GLIS1 : Intron Variant | AD |
rs6091723 | chr20:53661719 | G>A | SNV | Intergenic | AD |
rs825820 | chr10:53661544 | T>C | SNV | Intergenic | AD |
rs9416295 | chr10:53653356 | T>C | SNV | Intergenic | AD |
rs9416285 | chr10:53621431 | C>A / C>T | SNV | Intergenic | AD |
rs9416282 | chr10:53618908 | A>G | SNV | Intergenic | AD |
rs1489843 | chr10:53607809 | G>A | SNV | Intergenic | AD |
rs1380131 | chr14:53606140 | C>T | SNV | LOC105370504 : Intron Variant | AD |
rs7904493 | chr10:53605659 | C>A | SNV | Intergenic | AD |
rs1932011 | chr10:53597376 | A>C | SNV | Intergenic | AD |
rs2179545 | chr6:53597167 | T>C | SNV | Intergenic | AD |
rs6445588 | chr3:53596652 | C>T | SNV | CACNA1D : Intron Variant | ND |
rs351847 | chr10:53584952 | T>C | SNV | Intergenic | AD |
rs3120130 | chr10:53583694 | A>G | SNV | Intergenic | AD |
rs1298637 | chr1:53492930 | C>T | SNV | Intergenic | ND |
rs1296438 | chr1:53471504 | A>C / A>G | SNV | Intergenic | ND |
rs10429416 | chr8:53453931 | C>A | SNV | LOC100507516 : Intron Variant | ND |
rs9436924 | chr1:53447407 | C>T | SNV | Intergenic | ND |
rs9395865 | chr6:53442896 | C>T | SNV | Intergenic | AD |
rs16919143 | chr8:53418126 | C>A | SNV | LOC100507516 : Intron Variant | ND |
rs12147371 | chr14:53405676 | G>A | SNV | LOC105370504 : Intron Variant | AD |
rs10498449 | chr14:53399284 | C>G | SNV | LOC105370504 : Intron Variant | AD |
rs7718197 | chr5:53386186 | C>T | SNV | Intergenic | AD |
rs1416095 | chr1:53343021 | A>G | SNV | LOC105378731 : Intron Variant | AD |
rs3820198 | chr1:53326979 | A>C | SNV | LRP8 : Missense Variant LOC105378732 : 2KB Upstream Variant | AD |
rs1996017 | chr20:53306099 | T>C | SNV | TSHZ2 : Intron Variant | AD |
rs6022378 | chr20:53300709 | A>G | SNV | TSHZ2 : Intron Variant | AD |
rs1543080 | chr20:53280576 | C>A | SNV | TSHZ2 : Intron Variant | AD |
rs2281274 | chr6:53278756 | T>C | SNV | ELOVL5 : Intron Variant | AD |
rs200848948 | chr2:53266605-53266620 | delA / dupA | Indel | Intergenic | AD |
rs7170453 | chr15:53228348 | C>T | SNV | Intergenic | ND |
rs7615501 | chr3:53141541 | G>A | SNV | Intergenic | AD |
rs10423632 | chr19:53130297 | A>G | SNV | ZNF415 : Intron Variant | AD |
rs4356720 | chr20:53055771 | A>G | SNV | TSHZ2 : Intron Variant | AD |
rs910380 | chr20:53032939 | T>C | SNV | TSHZ2 : Intron Variant | AD |
rs2226194 | chr13:52981121 | C>T | SNV | Intergenic | AD |
rs4784281 | chr16:52970596 | A>T | SNV | Intergenic | AD |
rs17053117 | chr13:52969032 | G>A / G>T | SNV | Intergenic | AD |
rs2208989 | chr13:52953838 | C>T | SNV | Intergenic | AD |
rs371403 | chr6:52937446 | A>G | SNV | Intergenic | AD |
rs12930501 | chr16:52887867 | G>A | SNV | Intergenic | AD |
rs7201620 | chr16:52885164 | G>A | SNV | Intergenic | AD |
rs481440 | chr1:52879304 | C>T | SNV | ZYG11A : Intron Variant | AD |
rs10112899 | chr8:52846326 | G>A / G>C | SNV | Intergenic | AD |
rs10469016 | chr18:52800515 | G>A | SNV | DCC : Intron Variant | AD |
rs1579237 | chr16:52799510 | T>C | SNV | Intergenic | AD |
rs115714636 | chr3:52796511 | A>G | SNV | ITIH3 : Missense Variant | AD |
rs12312467 | chr12:52790941 | G>A | SNV | KRT3 : Intron Variant | ND |
rs9536287 | chr13:52785277 | G>A | SNV | Intergenic | AD |
rs235786 | chr13:52785150 | C>T | SNV | Intergenic | AD |
rs10515956 | chr18:52782062 | G>A | SNV | DCC : Intron Variant | AD |
rs7397684 | chr12:52779289 | A>G | SNV | KRT76 : 2KB Upstream Variant | AD |
rs1982266 | chr10:52770876 | A>G | SNV | MBL2 : Intron Variant | CD |
rs6508159 | chr18:52761650 | C>A / C>T | SNV | DCC : Intron Variant | AD |
rs10083941 | chr18:52755752 | C>T | SNV | DCC : Intron Variant | AD |
rs2433285 | chr15:52705779 | T>C | SNV | FAM214A : Intron Variant | AD |
rs115960994 | chr3:52697812 | C>T | SNV | GLT8D1 : Missense Variant | AD |
rs14024 | chr12:52675230 | T>C | SNV | KRT1 : Missense Variant | AD |
rs11715796 | chr3:52661634 | A>C | SNV | PBRM1 : Intron Variant | ND |
rs959781 | chr10:52640042 | C>T | SNV | LOC105378305 : Intron Variant | AD |
rs1007894 | chr14:52627877 | G>A | SNV | GPR137C : Intron Variant | AD |
rs1221884 | chr18:52608976 | A>G | SNV | DCC : Intron Variant | AD |
rs1221877 | chr18:52607456 | A>G | SNV | DCC : Intron Variant | AD |
rs670142 | chr12:52607203 | A>C | SNV | KRT73 : Intron Variant | CD |
rs1221874 | chr18:52604740 | A>G | SNV | DCC : Intron Variant | AD |
rs1221872 | chr18:52603967 | A>G | SNV | DCC : Intron Variant | AD |
rs10824650 | chr10:52602138 | A>G | SNV | LOC105378305 : Intron Variant | AD |
rs4901286 | chr14:52579883 | G>A | SNV | GPR137C : Intron Variant | AD |
rs804753 | chr7:52552937 | T>C / T>G | SNV | Intergenic | AD |
rs712013 | chr7:52544575 | G>A | SNV | Intergenic | AD |
rs8046979 | chr16:52521830 | A>G | SNV | TOX3 : Intron Variant | ND |
rs324119 | chr19:52396303 | C>A / C>G / C>T | SNV | ZNF528 : Intron Variant ZNF528-AS1 : Intron Variant | AD |
rs1125832 | chr16:52387228 | T>A | SNV | Intergenic | AD |
rs8008292 | chr14:52301846 | T>C | SNV | Intergenic | AD |
rs1729578 | chr10:52223498 | T>C / T>G | SNV | PRKG1 : Intron Variant | AD |
rs2154225 | chr6:52198303 | C>T | SNV | Intergenic | ND |
rs7829966 | chr8:52169257 | G>A | SNV | ST18 : Intron Variant | ND |
rs17290977 | chr8:52156360 | C>T | SNV | ST18 : Intron Variant | AD |
rs941612 | chr14:52154950 | A>G | SNV | Intergenic | AD |
rs3891723 | chr8:52146926 | G>A | SNV | ST18 : Intron Variant | AD |
rs7837915 | chr8:52145941 | G>A | SNV | ST18 : Intron Variant | AD |
rs7010548 | chr8:52142923 | C>T | SNV | ST18 : Intron Variant | AD |
rs3815868 | chr8:52136477 | T>C / T>G | SNV | ST18 : Intron Variant | AD |
rs11990195 | chr8:52134121 | G>A | SNV | ST18 : Intron Variant | AD |
rs9694119 | chr8:52128630 | T>C | SNV | ST18 : Intron Variant | AD |
rs7821217 | chr8:52127160 | G>A | SNV | ST18 : Intron Variant | AD |
rs2114226 | chr8:52124789 | T>C | SNV | ST18 : Intron Variant | AD |
rs42771 | chr16:52070835 | G>A | SNV | C16orf97 : Intron Variant | AD |
rs2450153 | chr8:52059112 | A>G | SNV | Intergenic | AD |
rs268928 | chr8:52055258 | A>G | SNV | Intergenic | AD |
rs33364 | chr16:52055223 | G>T | SNV | C16orf97 : Intron Variant | AD |
rs1592477 | chr16:52049779 | C>T | SNV | C16orf97 : Intron Variant | AD |
rs17641137 | chr10:52046842 | C>T | SNV | PRKG1 : Intron Variant | AD | ND |
rs2252399 | chr8:52039413 | A>C | SNV | Intergenic | AD |
rs256596 | chr16:52029000 | C>A | SNV | C16orf97 : Intron Variant | AD |
rs6021639 | chr20:52027936 | T>C | SNV | Intergenic | AD |
rs11076221 | chr16:51927631 | A>G | SNV | Intergenic | AD |
rs2842576 | chr1:51858556 | C>T | SNV | NRDC : Intron Variant | AD |
rs7080306 | chr10:51854153 | C>T | SNV | PRKG1 : Intron Variant | AD |
rs1937701 | chr10:51849217 | C>T | SNV | PRKG1 : Intron Variant | AD |
rs1417364 | chr1:51797410 | G>A | SNV | NRDC : Intron Variant LOC105378721 : Intron Variant | AD |
rs1004815 | chr1:51793053 | T>C / T>G | SNV | NRDC : Intron Variant LOC105378721 : 2KB Upstream Variant | AD |
rs11670215 | chr19:51684315 | T>G | SNV | Intergenic | AD |
rs4873568 | chr8:51644871 | T>C | SNV | PXDNL : Intron Variant | AD |
rs6493511 | chr15:51609408 | A>G | SNV | DMXL2 : Intron Variant | AD |
rs4687605 | chr3:51520026 | T>C | SNV | LOC105377085 : Intron Variant | AD |
rs3762714 | chr3:51483637 | G>A | SNV | VPRBP : Intron Variant | AD |
rs4687610 | chr3:51449194 | T>C | SNV | VPRBP : Intron Variant | AD |
rs17712228 | chr3:51440166 | G>A | SNV | VPRBP : Intron Variant | AD |
rs3749317 | chr3:51419581 | T>C | SNV | VPRBP : Intron Variant | AD |
rs2356261 | chr3:51407713 | C>A / C>G / C>T | SNV | VPRBP : Intron Variant | AD |
rs10510758 | chr3:51404233 | C>A | SNV | VPRBP : Intron Variant | AD |
rs3792408 | chr3:51400166 | A>G | SNV | VPRBP : Intron Variant | AD |
rs3804766 | chr3:51393226 | A>C | SNV | RBM15B : Synonymous Variant | AD |
rs2217938 | chr3:51388243 | A>G | SNV | MANF : Intron Variant | AD |
rs2304512 | chr3:51388050 | T>C | SNV | MANF : Intron Variant | AD |
rs1370124 | chr3:51384757 | A>G | SNV | MANF : 2KB Upstream Variant | AD |
rs2306431 | chr3:51356026 | C>T | SNV | DOCK3 : Intron Variant | AD |
rs4974096 | chr3:51355615 | G>A | SNV | DOCK3 : Intron Variant | AD |
rs17051755 | chr3:51349616 | T>C | SNV | DOCK3 : Intron Variant | AD |
rs7635095 | chr3:51345221 | C>T | SNV | DOCK3 : Intron Variant | AD |
rs7642077 | chr3:51345170 | T>C | SNV | DOCK3 : Intron Variant | AD |
rs7630259 | chr3:51341117 | G>A | SNV | DOCK3 : Intron Variant | AD |
rs10490975 | chr10:51261176 | G>A / G>T | SNV | PRKG1 : Intron Variant | AD |
rs7500931 | chr16:51245913 | T>C | SNV | Intergenic | AD |
rs10747608 | chr12:51222798 | A>G | SNV | Intergenic | AD |
rs17252296 | chr14:51114203 | A>C | SNV | Intergenic | ND |
rs4238821 | chr16:51110424 | T>C | SNV | Intergenic | AD |
rs11086322 | chr20:51098219 | G>A | SNV | Intergenic | ND |
rs10521221 | chr16:51096248 | C>T | SNV | Intergenic | AD |
rs8009082 | chr14:51032626 | C>A | SNV | TRIM9 : Intron Variant | ND |
rs10490162 | chr2:51020519 | T>C | SNV | NRXN1 : Intron Variant | ND |
rs13382584 | chr2:51020156 | T>C | SNV | NRXN1 : Intron Variant | AD |
rs12467557 | chr2:51015132 | A>G | SNV | NRXN1 : Intron Variant | ND |
rs12623467 | chr2:50997951 | C>T | SNV | NRXN1 : Intron Variant | ND |
rs60617249 | chr7:50944161 | A>G | SNV | Intergenic | AD |
rs198967 | chr19:50909765 | G>A | SNV | KLK4 : Intron Variant | AD |
rs198966 | chr19:50908754 | G>A | SNV | KLK4 : Synonymous Variant | AD |
rs2193225 | chr2:50852344 | T>C | SNV | NRXN1 : Intron Variant | ND |
rs17051404 | chr3:50714419 | A>C / A>G | SNV | DOCK3 : Intron Variant | AD |
rs11205760 | chr1:50708658 | C>T | SNV | FAF1 : Intron Variant | AD |
rs713179 | chr8:50700923 | A>G | SNV | SNTG1 : Intron Variant | AD |
rs7173321 | chr15:50630403 | C>G | SNV | TRPM7 : Intron Variant | ND |
rs2190498 | chr7:50621817 | A>G | SNV | GRB10 : Intron Variant | AD |
rs2232251 | chr3:50577559 | T>C / T>G | SNV | HEMK1 : Missense Variant | AD |
rs921451 | chr7:50555587 | T>C | SNV | DDC : Intron Variant | ND |
rs930707 | chr7:50551980 | A>G | SNV | DDC : Intron Variant | AD |
rs11575302 | chr7:50539996 | G>A | SNV | DDC : Synonymous Variant DDC-AS1 : Non Coding Transcript Variant | AD |
rs5770871 | chr22:50539833 | G>A | SNV | LOC102724608 : 2KB Upstream Variant | AD |
rs3735273 | chr7:50529166 | C>T | SNV | DDC : Intron Variant | ND |
rs11575340 | chr7:50528773 | G>A / G>T | SNV | DDC : Intron Variant | AD |
rs12487817 | chr3:50525135 | T>C | SNV | Intergenic | AD |
rs10940335 | chr5:50502595 | T>C | SNV | Intergenic | AD |
rs1016620 | chr5:50490763 | A>G | SNV | Intergenic | AD |
rs6721498 | chr2:50485874 | G>A | SNV | NRXN1 : Intron Variant | ND |
rs1451371 | chr7:50485353 | T>C | SNV | DDC : Intron Variant | ND |
rs3827730 | chr1:50472176 | T>C | SNV | FAF1 : Intron Variant | AD |
rs7378969 | chr5:50471925 | T>C | SNV | Intergenic | AD |
rs11575522 | chr7:50467697 | C>T | SNV | DDC : Intron Variant | AD |
rs11575537 | chr7:50464187 | C>T | SNV | DDC : Intron Variant | AD |
rs11575542 | chr7:50463289 | C>T | SNV | DDC : Missense Variant | AD |
rs11575543 | chr7:50463171 | G>A | SNV | DDC : Intron Variant | AD |
rs11575549 | chr7:50462479 | C>A / C>G / C>T | SNV | DDC : Intron Variant | AD |
rs7720960 | chr5:50450489 | A>G | SNV | Intergenic | AD |
rs13157992 | chr5:50444074 | C>T | SNV | EMB : 2KB Upstream Variant | AD |
rs4381241 | chr1:50441766 | T>C | SNV | FAF1 : Intron Variant | AD |
rs1278530 | chr1:50423583 | G>A | SNV | DMRTA2 : 2KB Upstream Variant LOC105378714 : Non Coding Transcript Variant | AD |
rs7792486 | chr7:50418611 | T>A / T>C | SNV | Intergenic | AD |
rs1278537 | chr1:50416487 | G>T | SNV | Intergenic | AD |
rs2036902 | chr5:50401098 | A>G | SNV | EMB : Intron Variant | AD |
rs7612641 | chr3:50393047 | G>A | SNV | CACNA2D2 : Intron Variant | AD |
rs7644782 | chr3:50387383 | A>G | SNV | CACNA2D2 : Intron Variant | AD |
rs10042504 | chr5:50386329 | A>G | SNV | Intergenic | AD |
rs12874278 | chr13:50361786 | C>T | SNV | DLEU1 : Intron Variant | ND |
rs3862266 | chr1:50356763 | G>A | SNV | Intergenic | AD |
rs7710841 | chr5:50349986 | C>T | SNV | Intergenic | AD |
rs10064702 | chr5:50336928 | T>G | SNV | Intergenic | AD |
rs1008509 | chr17:50328890 | T>C | SNV | Intergenic | ND |
rs928072 | chr20:50318241 | A>G | SNV | LINC01271 : Intron Variant | ND |
rs7269352 | chr20:50301883 | A>G | SNV | LINC01270 : Intron Variant | AD |
rs2813323 | chr10:50279397 | G>A | SNV | Intergenic | AD |
rs4865676 | chr5:50279343 | A>C / A>T | SNV | Intergenic | AD |
rs1674512 | chr5:50268794 | G>A | SNV | Intergenic | AD |
rs2049675 | chr17:50257586 | C>T | SNV | LOC105371822 : Non Coding Transcript Variant | AD |
rs11004819 | chr10:50253880 | C>T | SNV | Intergenic | OD |
rs1898198 | chr10:50249888 | A>G | SNV | ASAH2 : Intron Variant | OD |
rs11670669 | chr19:50248541 | G>A | SNV | MYH14 : Intron Variant | ND |
rs559096 | chr5:50226512 | C>T | SNV | Intergenic | AD |
rs7293378 | chr5:50192402 | G>A | SNV | Intergenic | AD |
rs1365507 | chr15:50185038 | A>G | SNV | SLC27A2 : Intron Variant | AD |
rs10273199 | chr7:50167951 | A>C | SNV | Intergenic | AD |
rs12531206 | chr7:50167936 | G>A | SNV | Intergenic | AD |
rs9436447 | chr1:50125060 | G>A | SNV | ELAVL4 : Intron Variant | AD |
rs9436444 | chr1:50124126 | G>A | SNV | ELAVL4 : Intron Variant | AD |
rs138229 | chr22:50118978 | A>G | SNV | MOV10L1 : Intron Variant | AD |
rs2624834 | chr3:50094698 | G>T | SNV | RBM5 : Intron Variant | AD |
rs3782323 | chr12:50089138 | G>A | SNV | SMARCD1 : Intron Variant | AD |
rs2240328 | chr3:50075571 | T>C | SNV | RBM6 : Intron Variant | AD |
rs8024393 | chr15:50060690 | A>G | SNV | ATP8B4 : Intron Variant | AD |
rs10422999 | chr19:50059963 | C>A | SNV | FLJ26850 : Intron Variant LOC100287477 : Missense Variant | AD |
rs4785201 | chr16:50055281 | A>G | SNV | Intergenic | AD |
rs137878 | chr22:50018362 | G>A | SNV | TTLL8 : 500B Downstream Variant | AD |
rs2624821 | chr3:49976681 | G>A | SNV | RBM6 : Intron Variant | AD |
rs2681779 | chr3:49973588 | T>C | SNV | RBM6 : Intron Variant | AD |
rs11681792 | chr2:49957256 | C>T | SNV | NRXN1 : Intron Variant | AD |
rs6504626 | chr17:49942527 | T>C | SNV | Intergenic | AD |
rs28460675 | chr22:49938357 | G>T | SNV | Intergenic | ND |
rs2290775 | chr19:49871985 | C>T | SNV | AKT1S1 : Intron Variant | ND |
rs2281223 | chr20:49867704 | G>A | SNV | SLC9A8 : Intron Variant | AD |
rs17786105 | chr20:49850348 | A>G | SNV | SLC9A8 : Intron Variant | AD |
rs4809760 | chr20:49838134 | A>G | SNV | SLC9A8 : Intron Variant | AD |
rs752522 | chr19:49835196 | C>G / C>T | SNV | MED25 : Intron Variant | ND |
rs8118160 | chr20:49818099 | A>G | SNV | SLC9A8 : Intron Variant | AD |
rs2286948 | chr19:49813497 | C>T | SNV | FUZ : Intron Variant | AD |
rs4916992 | chr7:49793276 | T>G | SNV | VWC2 : Intron Variant | ND |
rs6067212 | chr20:49764513 | C>T | SNV | LOC105372652 : 500B Downstream Variant | AD |
rs74745534 | chr6:49589080 | C>T | SNV | Intergenic | AD |
rs7238552 | chr18:49511029 | C>T | SNV | LOC101928144 : Intron Variant | AD |
rs7148751 | chr14:49402182 | G>A | SNV | Intergenic | AD |
rs16948058 | chr17:49372137 | C>T | SNV | LOC102724596 : Intron Variant | AD |
rs4898519 | chr12:49320320 | A>G / A>T | SNV | TROAP : 2KB Upstream Variant LOC101927267 : Intron Variant | AD |
rs1177825 | chr19:49235225 | C>T | SNV | LOC107985340 : Intron Variant | AD |
rs7772532 | chr6:48990205 | T>G | SNV | Intergenic | AD |
rs742977 | chr22:48982682 | G>A | SNV | Intergenic | ND |
rs9367338 | chr6:48982301 | C>T | SNV | Intergenic | AD |
rs1420585 | chr16:48961985 | C>T | SNV | Intergenic | AD |
rs8031813 | chr15:48961764 | C>A / C>T | SNV | SHC4 : Intron Variant | AD |
rs989373 | chr2:48931186 | T>C | SNV | Intergenic | AD |
rs12953717 | chr18:48927559 | C>T | SNV | SMAD7 : Intron Variant | AD |
rs9357585 | chr6:48895241 | G>A | SNV | Intergenic | AD |
rs1938218 | chr6:48890842 | T>C | SNV | Intergenic | AD |
rs885685 | chr7:48888701 | G>A | SNV | Intergenic | AD |
rs11631496 | chr15:48783721 | T>C | SNV | CEP152 : Intron Variant LOC101928472 : 2KB Upstream Variant | AD |
rs6010529 | chr22:48781929 | A>G | SNV | Intergenic | AD |
rs2413913 | chr15:48718852 | C>T | SNV | CEP152 : Intron Variant | AD |
rs7297499 | chr12:48706067 | T>C | SNV | CCNT1 : Intron Variant | AD |
rs9909854 | chr17:48679529 | C>T | SNV | LOC105371809 : Intron Variant | AD |
rs2898086 | chr12:48675853 | T>C | SNV | KANSL2 : Intron Variant | AD |
rs5771934 | chr22:48673638 | T>C | SNV | FAM19A5 : Intron Variant | ND |
rs7315319 | chr12:48673157 | T>C | SNV | KANSL2 : Intron Variant | AD |
rs16999684 | chr22:48671066 | A>C | SNV | FAM19A5 : Intron Variant | ND |
rs13250857 | chr8:48583594 | G>A | SNV | LOC101929268 : Intron Variant | AD |
rs10504065 | chr8:48572345 | C>T | SNV | LOC101929268 : Intron Variant | AD |
rs7944287 | chr11:48495054 | T>C | SNV | Intergenic | ND |
rs13280598 | chr8:48452320 | C>A | SNV | LOC105375821 : Intron Variant | AD |
rs8082814 | chr18:48450704 | G>A / G>T | SNV | Intergenic | AD |
rs544475121 | chr13:48442207-48442218 | delT | Indel | LPAR6 : Intron Variant RB1 : Intron Variant | AD |
rs34997741 | chr19:48432396 | T>C | SNV | GRIN2D : Intron Variant | AD |
rs6987448 | chr8:48410825 | C>T | SNV | LOC105375821 : Intron Variant | AD |
rs4858818 | chr3:48408675 | C>T | SNV | PLXNB1 : Intron Variant | AD |
rs3745720 | chr19:48332825 | A>C | SNV | TMEM143 : Non Coding Transcript Variant | AD |
rs9957779 | chr18:48291377 | A>G | SNV | ZBTB7C : Intron Variant | AD |
rs169439 | chr10:48242632 | C>A | SNV | FRMPD2 : Intron Variant | ND |
rs10500299 | chr19:48218923 | C>T | SNV | CARD8 : Synonymous Variant | AD |
rs12624655 | chr20:48176216 | G>A / G>T | SNV | Intergenic | AD |
rs60630422 | chr20:48174246 | C>A / C>T | SNV | Intergenic | AD |
rs62202398 | chr20:48172481 | G>A / G>C | SNV | Intergenic | AD |
rs3731539 | chr3:48167996 | C>T | SNV | CDC25A : Intron Variant | AD |
rs6507820 | chr18:48167910 | C>A / C>T | SNV | ZBTB7C : Intron Variant LOC105372104 : Intron Variant | AD |
rs4939747 | chr18:48162470 | C>T | SNV | ZBTB7C : Intron Variant LOC105372104 : Non Coding Transcript Variant | AD |
rs17198978 | chr11:48150813 | C>T | SNV | PTPRJ : Intron Variant | ND |
rs6463462 | chr7:48102597 | G>T | SNV | UPP1 : Intron Variant | ND |
rs9316348 | chr13:48092554 | G>A | SNV | MED4 : Intron Variant | AD |
rs6485806 | chr11:48081254 | C>T | SNV | PTPRJ : Intron Variant | AD |
rs6755400 | chr2:48073712 | A>G | SNV | Intergenic | ND |
rs737791 | chr22:48061879 | G>A | SNV | Intergenic | AD |
rs1014674 | chr22:48057849 | C>A / C>T | SNV | Intergenic | AD |
rs9595835 | chr13:48054313 | T>C | SNV | Intergenic | AD |
rs4794333 | chr17:47968129 | T>C | SNV | CDK5RAP3 : Intron Variant | ND |
rs7936879 | chr11:47955330 | A>G | SNV | Intergenic | ND |
rs34675858 | chr3:47860757 | C>T | SNV | MAP4 : Intron Variant | AD |
rs878487 | chr22:47781367 | A>G | SNV | LOC284930 : Intron Variant | AD |
rs4245815 | chr2:47592833 | G>A | SNV | MSH2 : Intron Variant | AD |
rs334524 | chr7:47526559 | A>T | SNV | TNS3 : Intron Variant | AD |
rs830140 | chr19:47444725 | A>G | SNV | SLC8A2 : Intron Variant | AD |
rs698705 | chr19:47434209 | A>G | SNV | SLC8A2 : Intron Variant | OD |
rs6018477 | chr20:47431079 | A>C | SNV | Intergenic | AD |
rs7090464 | chr10:47385686 | A>G / A>T | SNV | ZNF488 : 2KB Upstream Variant | AD |
rs3905310 | chr6:47351082 | G>A | SNV | Intergenic | AD |
rs6122571 | chr20:47277392 | T>C | SNV | ZMYND8 : Intron Variant | AD |
rs11090754 | chr22:47275457 | T>C | SNV | Intergenic | ND |
rs11704468 | chr22:47263264 | C>T | SNV | Intergenic | AD |
rs6463401 | chr7:47243291 | G>A | SNV | Intergenic | ND |
rs9828473 | chr3:47118198 | G>A | SNV | SETD2 : Intron Variant | AD |
rs9727862 | chr1:47015944 | G>A | SNV | CYP4X1 : Intron Variant | AD |
rs16941404 | chr17:46976814 | C>G | SNV | Intergenic | ND |
rs2903517 | chr11:46945257 | G>A | SNV | C11orf49 : Intron Variant | ND |
rs6018185 | chr20:46928812 | T>C | SNV | EYA2 : Intron Variant | AD |
rs6066110 | chr20:46911158 | A>G | SNV | EYA2 : Intron Variant | AD |
rs6910089 | chr6:46904248 | T>C | SNV | ADGRF5 : Intron Variant LOC101926962 : Intron Variant | ND |
rs16859614 | chr4:46892510 | C>T | SNV | COX7B2 : Intron Variant | AD |
rs1004018 | chr6:46886666 | G>A | SNV | ADGRF5 : Intron Variant | ND |
rs3092084 | chr20:46833227 | C>T | SNV | Intergenic | ND |
rs6793661 | chr3:46736518 | C>T | SNV | PRSS46 : 2KB Upstream Variant | AD |
rs6808303 | chr3:46736395 | T>C | SNV | PRSS46 : 5 Prime UTR Variant | AD |
rs7639979 | chr3:46733286 | A>G | SNV | PRSS46 : Intron Variant | AD |
rs3799861 | chr6:46721792 | T>C | SNV | PLA2G7 : Intron Variant | AD |
rs3786704 | chr19:46721333 | C>T | SNV | STRN4 : Intron Variant LOC107987269 : 2KB Upstream Variant | AD |
rs10412340 | chr19:46718501 | G>A | SNV | PRKD2 : 2KB Upstream Variant LOC107987269 : Synonymous Variant | AD |
rs12528857 | chr6:46702199 | C>A | SNV | PLA2G7 : Non Coding Transcript Variant TDRD6 : 3 Prime UTR Variant | AD |
rs12229299 | chr12:46691110 | C>A / C>G | SNV | Intergenic | AD |
rs11961117 | chr6:46686509 | G>A | SNV | TDRD6 : 2KB Upstream Variant LOC101926934 : Intron Variant | AD |
rs12608819 | chr19:46662617 | C>T | SNV | DACT3-AS1 : Intron Variant DACT3 : 2KB Upstream Variant | AD |
rs10807344 | chr6:46657898 | C>T | SNV | SLC25A27 : Intron Variant | AD |
rs1933932 | chr1:46643656 | C>T | SNV | ATPAF1 : Intron Variant | AD |
rs544049 | chr18:46624750 | G>A | SNV | LOXHD1 : Intron Variant | AD |
rs875778 | chr22:46588409 | T>C | SNV | GRAMD4 : Intron Variant | AD |
rs16995232 | chr22:46421424 | A>G | SNV | CELSR1 : Intron Variant | ND |
rs7293345 | chr5:46332281 | C>T | SNV | Intergenic | AD |
rs4975962 | chr5:46284752 | C>T | SNV | Intergenic | AD |
rs4803913 | chr19:46265496 | A>G | SNV | Intergenic | AD |
rs11958464 | chr5:46211801 | C>T | SNV | Intergenic | AD |
rs912784 | chr13:46211386 | C>A | SNV | LRRC63 : 2KB Upstream Variant LOC107984578 : Non Coding Transcript Variant | AD |
rs7293423 | chr5:46192118 | G>A | SNV | Intergenic | AD |
rs9567638 | chr13:46180599 | T>C | SNV | LCP1 : Intron Variant | AD |
rs8185226 | chr5:46160685 | T>C | SNV | Intergenic | AD |
rs2345955 | chr2:46093741 | C>T | SNV | PRKCE : Intron Variant | ND |
rs6074015 | chr20:46083536 | C>T | SNV | NCOA5 : Intron Variant | AD |
rs1470598 | chr2:46042428 | A>G | SNV | PRKCE : Intron Variant | ND |
rs17178655 | chr10:46034023 | C>T | SNV | MSMB : Intron Variant LOC105378287 : Intron Variant | ND |
rs4293630 | chr21:46025877 | A>G | SNV | Intergenic | AD |
rs4714899 | chr6:45979730 | G>A | SNV | CLIC5 : Intron Variant | ND |
rs2595211 | chr2:45979613 | T>A / T>G | SNV | PRKCE : Intron Variant | ND |
rs3777599 | chr6:45975213 | G>T | SNV | CLIC5 : Intron Variant | ND |
rs11038720 | chr11:45947110 | A>T | SNV | PHF21A : Intron Variant | AD |
rs4810479 | chr20:45916409 | C>T | SNV | Intergenic | AD |
rs1553009 | chr7:45869395 | G>A | SNV | Intergenic | AD |
rs12667301 | chr7:45867304 | G>A | SNV | Intergenic | AD |
rs6680211 | chr1:45849335 | C>G | SNV | MAST2 : Intron Variant | ND |
rs7284693 | chr22:45817711 | A>G | SNV | ATXN10 : Intron Variant | AD |
rs4900680 | chr14:45798982 | A>G | SNV | Intergenic | AD |
rs1686312 | chr14:45772294 | G>A / G>T | SNV | LOC105370478 : Intron Variant | AD |
rs1266294 | chr14:45763651 | A>C | SNV | LOC105370478 : Intron Variant | AD |
rs462145 | chr20:45749572 | A>G | SNV | WFDC3 : Intron Variant | AD |
rs7243707 | chr18:45652309 | A>C | SNV | SLC14A2 : Intron Variant LOC105372093 : Intron Variant | AD |
rs1348965 | chr11:45642018 | T>C | SNV | Intergenic | AD |
rs12622230 | chr2:45628176 | A>C | SNV | Intergenic | AD |
rs16979890 | chr19:45563060 | G>A | SNV | OPA3 : Intron Variant | AD |
rs1264226 | chr19:45559909 | G>A | SNV | OPA3 : Intron Variant | AD |
rs73135175 | chr4:45545051 | C>T | SNV | Intergenic | AD |
rs8111589 | chr19:45531300 | C>T | SNV | OPA3 : Intron Variant | AD |
rs8099273 | chr18:45524247 | A>G | SNV | SLC14A2 : Intron Variant | AD |
rs8099211 | chr18:45523993 | G>A | SNV | SLC14A2 : Intron Variant | AD |
rs9614670 | chr22:45442936 | C>T | SNV | Intergenic | AD |
rs1321075 | chr6:45424206 | T>G | SNV | RUNX2 : Intron Variant | AD |
rs9614466 | chr22:45415482 | A>G | SNV | RIBC2 : Intron Variant SMC1B : 2KB Upstream Variant | AD |
rs2216506 | chr2:45408326 | T>C | SNV | SRBD1 : Intron Variant | AD |
rs6874279 | chr5:45393159 | G>A | SNV | HCN1 : Intron Variant | AD |
rs10167668 | chr2:45355180 | A>G | SNV | Intergenic | ND |
rs4245803 | chr2:45347067 | G>A | SNV | Intergenic | AD |
rs34993366 | chr17:45326782 | T>C | SNV | Intergenic | AD |
rs7965430 | chr12:45316447 | A>G | SNV | ANO6 : Intron Variant | AD |
rs344797 | chr19:45304884 | T>G | SNV | MARK4 : 3 Prime UTR Variant | AD |
rs7138247 | chr12:45275970 | G>A | SNV | ANO6 : Intron Variant | AD |
rs1938407 | chr1:45256950 | A>G | SNV | Intergenic | CD |
rs2052603 | chr12:45252483 | G>T | SNV | ANO6 : Intron Variant | AD |
rs33786 | chr3:45251887 | G>A | SNV | Intergenic | AD |
rs33779 | chr3:45247042 | T>C | SNV | Intergenic | AD |
rs2997460 | chr1:45229124 | C>T | SNV | Intergenic | CD |
rs1938300 | chr1:45207111 | T>C | SNV | ZSWIM5 : 2KB Upstream Variant | CD |
rs12231753 | chr12:45203757 | C>T | SNV | PLEKHA8P1 : Intron Variant | AD |
rs11125007 | chr2:45198965 | G>A | SNV | LINC01121 : Intron Variant | CD |
rs3788164 | chr21:45136301 | T>C | SNV | ADARB1 : Intron Variant | AD |
rs2301597 | chr17:45095905 | T>C | SNV | NMT1 : Intron Variant | AD |
rs2959236 | chr2:45085828 | T>C | SNV | Intergenic | AD |
rs11211074 | chr1:45064837 | T>C | SNV | ZSWIM5 : Intron Variant | CD |
rs3850855 | chr1:45058221 | T>C | SNV | ZSWIM5 : Intron Variant | CD |
rs10514712 | chr3:45042436 | T>C | SNV | Intergenic | ND |
rs7731099 | chr5:45037924 | G>A | SNV | Intergenic | AD |
rs6007413 | chr22:45034435 | C>G | SNV | Intergenic | ND |
rs11848799 | chr14:44946394 | T>C | SNV | KLHL28 : Intron Variant | AD |
rs6007397 | chr22:44943320 | C>T | SNV | PHF21B : Intron Variant | AD |
rs528301 | chr2:44927769 | G>A | SNV | Intergenic | ND |
rs9463046 | chr6:44834981 | T>C | SNV | SUPT3H : Intron Variant LOC107986600 : Non Coding Transcript Variant | AD |
rs16992796 | chr22:44787134 | A>G | SNV | ARHGAP8 : Intron Variant PRR5-ARHGAP8 : Intron Variant | AD |
rs17115446 | chr14:44720499 | T>C | SNV | Intergenic | AD |
rs17115444 | chr14:44719763 | T>C | SNV | Intergenic | AD |
rs3759871 | chr15:44651559 | A>G | SNV | SPG11 : Missense Variant | AD |
rs12896581 | chr14:44640950 | C>A | SNV | Intergenic | AD |
rs6923772 | chr6:44565574 | A>G | SNV | Intergenic | AD |
rs1552859 | chr12:44537118 | G>T | SNV | NELL2 : Intron Variant | AD |
rs4768555 | chr12:44533557 | A>G | SNV | NELL2 : Intron Variant | AD |
rs2556560 | chr15:44529645 | A>G | SNV | Intergenic | AD |
rs1067344 | chr2:44393671 | T>G | SNV | CAMKMT : Intron Variant | AD |
rs4142248 | chr19:44384114 | T>C | SNV | Intergenic | AD |
rs11856569 | chr15:44382642 | A>C | SNV | CASC4 : Intron Variant | AD |
rs2014530 | chr22:44361191 | C>T | SNV | Intergenic | AD |
rs8024461 | chr15:44290688 | G>A | SNV | CASC4 : Intron Variant | AD |
rs2053458 | chr2:44215940 | C>G | SNV | PPM1B : Intron Variant | AD |
rs7280236 | chr21:44175177 | C>T | SNV | LOC105377139 : Non Coding Transcript Variant | AD |
rs2017246 | chr20:44147203 | A>G | SNV | JPH2 : Intron Variant | AD |
rs882020 | chr7:44139144 | C>T | SNV | MYL7 : Intron Variant | AD |
rs1236716 | chr19:44136776 | G>A | SNV | Intergenic | AD |
rs1236715 | chr19:44135405 | C>A / C>G | SNV | Intergenic | AD |
rs10413195 | chr19:44130750 | A>G | SNV | ZNF225 : Intron Variant | AD |
rs10413511 | chr19:44130658 | G>A | SNV | ZNF225 : Intron Variant | AD |
rs9304638 | chr19:44129933 | C>G / C>T | SNV | ZNF225 : Intron Variant | AD |
rs10406335 | chr19:44129800 | G>A | SNV | ZNF225 : Intron Variant | AD |
rs2284981 | chr19:44129405 | G>C | SNV | ZNF225 : Intron Variant | AD |
rs2284980 | chr19:44129321 | T>C | SNV | ZNF225 : Intron Variant | AD |
rs2168778 | chr19:44127066 | T>C | SNV | ZNF225 : Intron Variant | AD |
rs7508762 | chr19:44125725 | T>C | SNV | ZNF225 : Intron Variant | AD |
rs10853771 | chr19:44125295 | C>T | SNV | ZNF225 : Intron Variant | AD |
rs7251868 | chr19:44124204 | G>A | SNV | ZNF225 : Intron Variant | AD |
rs4802208 | chr19:44123759 | G>C | SNV | ZNF225 : Intron Variant | AD |
rs79605584 | chr17:44122308 | G>A | SNV | HDAC5 : Intron Variant | CD |
rs2356750 | chr19:44121756 | G>A | SNV | ZNF225 : Intron Variant | AD |
rs7253485 | chr19:44120889 | A>G | SNV | ZNF225 : Intron Variant | AD |
rs8099869 | chr19:44119223 | C>T | SNV | ZNF225 : Intron Variant | AD |
rs2300962 | chr19:44116050 | C>T | SNV | ZNF225 : Intron Variant | AD |
rs2284978 | chr19:44113157 | A>G | SNV | ZNF225 : Intron Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs2061333 | chr19:44110055 | C>T | SNV | ZNF225 : 2KB Upstream Variant ZNF224 : 500B Downstream Variant LOC100379224 : Intron Variant | AD |
rs2061332 | chr19:44109508 | A>C | SNV | ZNF224 : 3 Prime UTR Variant ZNF225 : 2KB Upstream Variant LOC100379224 : Intron Variant | AD |
rs6509141 | chr19:44108966 | C>T | SNV | ZNF224 : 3 Prime UTR Variant LOC100379224 : Intron Variant | AD |
rs3746319 | chr19:44108078 | A>G | SNV | ZNF224 : Missense Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs3200505 | chr19:44107861 | A>T | SNV | ZNF224 : Synonymous Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs3746321 | chr19:44107852 | A>G | SNV | ZNF224 : Synonymous Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs4508518 | chr19:44107267 | A>G / A>T | SNV | ZNF224 : Missense Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs4239529 | chr19:44106645 | A>T | SNV | ZNF224 : Missense Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs2068061 | chr19:44106512 | A>G | SNV | ZNF224 : Missense Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs7250171 | chr19:44106152 | C>T | SNV | ZNF224 : Intron Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs7250076 | chr19:44106142 | A>G | SNV | ZNF224 : Intron Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs7249834 | chr19:44105942 | A>G | SNV | ZNF224 : Intron Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs7249827 | chr19:44105876 | C>A | SNV | ZNF224 : Intron Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs3172 | chr19:44105693 | C>G | SNV | ZNF224 : Intron Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs8101657 | chr19:44105571 | T>A | SNV | ZNF224 : Intron Variant LOC100379224 : Non Coding Transcript Variant | AD |
rs4803681 | chr19:44105332 | G>A / G>C | SNV | ZNF224 : Intron Variant LOC100379224 : 500B Downstream Variant | AD |
rs4803680 | chr19:44105140 | T>C | SNV | ZNF224 : Intron Variant LOC100379224 : 500B Downstream Variant | AD |
rs4803679 | chr19:44105007 | A>T | SNV | ZNF224 : Intron Variant LOC100379224 : 500B Downstream Variant | AD |
rs4803678 | chr19:44104994 | C>T | SNV | ZNF224 : Intron Variant LOC100379224 : 500B Downstream Variant | AD |
rs4803677 | chr19:44104810 | C>T | SNV | ZNF224 : Intron Variant | AD |
rs8113750 | chr19:44104636 | C>T | SNV | ZNF224 : Intron Variant | AD |
rs10420143 | chr19:44103929 | A>G | SNV | ZNF224 : Intron Variant | AD |
rs28446946 | chr19:44103466 | T>C | SNV | ZNF224 : Intron Variant | AD |
rs28539456 | chr19:44103394 | G>T | SNV | ZNF224 : Intron Variant | AD |
rs8105860 | chr19:44102775 | A>G | SNV | ZNF224 : Intron Variant | AD |
rs4803676 | chr19:44100970 | G>A | SNV | ZNF224 : Intron Variant | AD |
rs62115526 | chr19:44100761 | T>C | SNV | ZNF224 : Intron Variant | AD |
rs8108404 | chr19:44099822 | G>T | SNV | ZNF224 : Intron Variant | AD |
rs8104573 | chr19:44099232 | A>G | SNV | ZNF224 : Intron Variant | AD |
rs7250004 | chr19:44098839 | A>G | SNV | ZNF224 : Intron Variant | AD |
rs7250005 | chr19:44098806 | C>T | SNV | ZNF224 : Intron Variant | AD |
rs10410306 | chr19:44097384 | T>C | SNV | ZNF224 : Intron Variant | AD |
rs4802207 | chr19:44096224 | C>T | SNV | ZNF224 : Intron Variant | AD |
rs4802206 | chr19:44096083 | C>T | SNV | ZNF224 : Intron Variant | AD |
rs4459653 | chr19:44095462 | C>T | SNV | ZNF224 : Intron Variant | AD |
rs4429390 | chr19:44094715 | T>G | SNV | ZNF224 : Intron Variant | AD |
rs4802205 | chr19:44093276 | G>A | SNV | ZNF224 : 2KB Upstream Variant | AD |
rs4802204 | chr19:44093142 | C>A | SNV | ZNF224 : 2KB Upstream Variant | AD |
rs8108021 | chr19:44091269 | A>G | SNV | Intergenic | AD |
rs62115524 | chr19:44088782 | A>G | SNV | ZNF284 : 3 Prime UTR Variant | AD |
rs56353321 | chr19:44088250 | T>C | SNV | ZNF284 : 3 Prime UTR Variant | AD |
rs55876899 | chr19:44088049 | C>T | SNV | ZNF284 : 3 Prime UTR Variant | AD |
rs8113487 | chr19:44087401 | G>A / G>C | SNV | ZNF284 : 3 Prime UTR Variant | AD |
rs8113249 | chr19:44087207 | G>A | SNV | ZNF284 : Missense Variant | AD |
rs57895932 | chr19:44076605 | T>C | SNV | ZNF284 : Intron Variant | AD |
rs4550576 | chr19:44074294 | A>G | SNV | ZNF284 : Intron Variant | AD |
rs7252213 | chr19:44072710 | G>A | SNV | ZNF284 : Intron Variant | AD |
rs11666432 | chr19:44072149 | C>T | SNV | ZNF284 : 5 Prime UTR Variant | AD |
rs9646633 | chr19:44070874 | A>G | SNV | ZNF284 : 2KB Upstream Variant | AD |
rs751442 | chr1:44043879 | A>C | SNV | KLF17 : 2KB Upstream Variant | ND |
rs4587082 | chr5:44012370 | C>A | SNV | Intergenic | AD |
rs1362153 | chr1:44003359 | T>C | SNV | SLC6A9 : Intron Variant | AD |
rs11696193 | chr20:43896850 | A>G | SNV | Intergenic | AD |
rs12760274 | chr1:43783673 | A>G | SNV | ST3GAL3 : Intron Variant | AD |
rs285171 | chr20:43709235 | C>G | SNV | MYBL2 : Intron Variant | ND |
rs16940095 | chr17:43680558 | A>G | SNV | LOC105371786 : Intron Variant LOC107985085 : Intron Variant | AD |
rs11582876 | chr1:43597156 | C>T | SNV | PTPRF : Intron Variant | AD |
rs2393938 | chr10:43568364 | T>C | SNV | ZNF239 : Intron Variant | ND |
rs7894102 | chr10:43559519 | G>A | SNV | ZNF239 : Intron Variant | ND |
rs10793442 | chr10:43556371 | C>A | SNV | ZNF239 : 3 Prime UTR Variant | ND |
rs7893169 | chr10:43555267 | A>G | SNV | ZNF239 : 3 Prime UTR Variant | ND |
rs13226386 | chr7:43528505 | G>A / G>T | SNV | HECW1 : Intron Variant | AD |
rs3884613 | chr13:43511809 | T>C | SNV | ENOX1 : Intron Variant | AD |
rs9680399 | chr21:43451183 | G>A | SNV | LINC00319 : Non Coding Transcript Variant | AD |
rs2888312 | chr3:43443475 | G>A | SNV | ANO10 : Intron Variant | AD |
rs11710107 | chr3:43432422 | A>C | SNV | ANO10 : Intron Variant | AD |
rs3816766 | chr11:43427735 | T>C | SNV | TTC17 : Intron Variant | AD |
rs1323161 | chr13:43426495 | G>A / G>T | SNV | ENOX1 : Intron Variant | AD |
rs12857536 | chr13:43309468 | G>T | SNV | ENOX1 : Non Coding Transcript Variant | AD |
rs7117651 | chr11:43299328 | C>T | SNV | Intergenic | CD |
rs9533443 | chr13:43293604 | G>A / G>C | SNV | ENOX1 : Intron Variant | ND |
rs12874803 | chr13:43285188 | T>C | SNV | ENOX1 : Intron Variant | AD |
rs12523436 | chr5:43276367 | C>T | SNV | NIM1K : Intron Variant | AD |
rs17723330 | chr7:43247294 | G>A | SNV | HECW1 : Intron Variant | AD |
rs17172185 | chr7:43247240 | T>C | SNV | HECW1 : Intron Variant | AD |
rs10507519 | chr13:43240987 | C>T | SNV | ENOX1 : Intron Variant | AD |
rs930577 | chr13:43232753 | G>A | SNV | ENOX1 : Intron Variant | AD |
rs2289774 | chr13:43224212 | T>C | SNV | ENOX1 : Intron Variant | AD |
rs11086862 | chr20:43125961 | T>C | SNV | PTPRT : Intron Variant | AD |
rs135015 | chr22:43102155 | T>C | SNV | Intergenic | AD |
rs3805944 | chr6:43077724 | G>T | SNV | PTK7 : Intron Variant | AD |
rs1198394 | chr1:43074667 | G>A | SNV | Intergenic | AD |
rs382571 | chr17:43019464 | G>A | SNV | VAT1 : Intron Variant | AD |
rs429464 | chr17:43018881 | T>C | SNV | VAT1 : Intron Variant | AD |
rs3793023 | chr6:43015021 | A>C | SNV | MEA1 : Intron Variant KLHDC3 : Intron Variant | AD |
rs12404679 | chr1:42992787 | C>T | SNV | Intergenic | AD |
rs5991588 | chrX:42803678 | C>T | SNV | Intergenic | AD |
rs5964217 | chrX:42790277 | G>A | SNV | Intergenic | AD |
rs5964215 | chrX:42788753 | T>C | SNV | Intergenic | AD |
rs12915116 | chr15:42782482 | C>T | SNV | TTBK2 : Intron Variant | AD |
rs11915803 | chr3:42758799 | T>C | SNV | CCDC13 : Intron Variant | AD |
rs7287569 | chr22:42757140 | C>A | SNV | Intergenic | AD |
rs7166775 | chr15:42750492 | G>A | SNV | TTBK2 : Intron Variant | AD |
rs55828312 | chr8:42734459 | A>G | SNV | CHRNB3 : Intron Variant | ND |
rs7331929 | chr13:42720353 | A>G | SNV | Intergenic | AD |
rs11037018 | chr11:42701037 | C>A | SNV | Intergenic | AD |
rs4924694 | chr15:42698868 | T>A | SNV | STARD9 : Intron Variant | AD |
rs6474412 | chr8:42695355 | C>T | SNV | Intergenic | ND |
rs13277524 | chr8:42694914 | G>T | SNV | Intergenic | ND |
rs13277254 | chr8:42694839 | G>A | SNV | Intergenic | ND |
rs1955185 | chr8:42694504 | C>T | SNV | Intergenic | ND |
rs3747193 | chr22:42692457 | G>T | SNV | A4GALT : 3 Prime UTR Variant | AD |
rs1451240 | chr8:42691568 | A>G | SNV | Intergenic | ND |
rs736013 | chr22:42688607 | T>C | SNV | Intergenic | AD |
rs17003212 | chr22:42683748 | T>C | SNV | Intergenic | AD |
rs4421732 | chr11:42678122 | A>G | SNV | Intergenic | AD |
rs7114882 | chr11:42641807 | T>C | SNV | Intergenic | AD |
rs1889310 | chr10:42486247 | A>T | SNV | LINC00839 : Intron Variant | AD |
rs11082277 | chr18:42470398 | G>A | SNV | LINC00907 : Intron Variant | ND |
rs1499378 | chr14:42461113 | C>T | SNV | Intergenic | AD |
rs17113034 | chr14:42439810 | T>C | SNV | Intergenic | AD |
rs7157217 | chr14:42438244 | C>T | SNV | Intergenic | AD |
rs928302 | chr21:42389975 | C>T | SNV | TMPRSS3 : Missense Variant | ND |
rs9839267 | chr3:42291132 | T>A / T>G | SNV | Intergenic | AD |
rs3788007 | chr21:42286666 | G>A | SNV | ABCG1 : Intron Variant | AD |
rs12366192 | chr11:42283513 | T>C | SNV | Intergenic | AD |
rs9879040 | chr3:42230626 | A>G / A>T | SNV | Intergenic | AD |
rs12364934 | chr11:42225911 | T>G | SNV | LOC100507205 : Intron Variant | AD |
rs1043610 | chr3:42224142 | C>G / C>T | SNV | TRAK1 : Non Coding Transcript Variant | AD |
rs3774391 | chr3:42223877 | C>T | SNV | TRAK1 : Non Coding Transcript Variant | AD |
rs11928109 | chr3:42217807 | G>A | SNV | TRAK1 : Intron Variant | AD |
rs6955604 | chr7:42217285 | G>C | SNV | GLI3 : Intron Variant | ND |
rs2154294 | chr14:42186072 | A>G | SNV | Intergenic | AD |
rs4234445 | chr3:42184659 | T>C | SNV | TRAK1 : Intron Variant | AD |
rs10135407 | chr14:42175414 | A>G | SNV | Intergenic | AD |
rs8006978 | chr14:42164869 | G>T | SNV | Intergenic | AD |
rs1356410 | chr15:42142639 | T>C | SNV | PLA2G4F : Missense Variant | AD |
rs6733455 | chr2:42123347 | C>T | SNV | Intergenic | AD |
rs3801187 | chr7:42116764 | G>A | SNV | GLI3 : Intron Variant | ND |
rs1542668 | chr14:42079709 | A>G | SNV | Intergenic | AD |
rs1684693 | chr14:42079054 | T>G | SNV | Intergenic | AD |
rs1668589 | chr15:42071571 | A>G | SNV | PLA2G4D : Intron Variant | AD |
rs17114247 | chr21:42058026 | C>T | SNV | Intergenic | ND |
rs1632694 | chr14:42042644 | C>T | SNV | Intergenic | AD |
rs1684716 | chr14:42028828 | T>A / T>G | SNV | Intergenic | AD |
rs11702690 | chr21:41987559 | A>G | SNV | ZBTB21 : 3 Prime UTR Variant | AD |
rs11620406 | chr13:41986636 | C>T | SNV | LOC105370176 : Intron Variant | AD |
rs1648811 | chr15:41930192 | A>G | SNV | EHD4 : Intron Variant | ND |
rs1536701 | chr6:41902186 | G>A | SNV | Intergenic | ND |
rs12441018 | chr15:41901373 | T>G | SNV | EHD4 : Intron Variant | CD |
rs1672461 | chr15:41897998 | C>T | SNV | LOC105370792 : Intron Variant | AD |
rs1197701 | chr15:41895294 | T>C / T>G | SNV | SPTBN5 : 2KB Upstream Variant LOC105370792 : Non Coding Transcript Variant | ND |
rs6972429 | chr7:41855244 | C>T | SNV | LOC107986788 : Intron Variant | ND |
rs17498875 | chr17:41853703 | C>G / C>T | SNV | KLHL11 : Non Coding Transcript Variant | AD |
rs29684 | chr7:41815054 | G>A | SNV | LOC107986788 : Intron Variant | ND |
rs7251960 | chr19:41802111 | C>T | SNV | CEACAM3 : Intron Variant | AD |
rs2701 | chr19:41771194 | G>A | SNV | CEACAM6 : 3 Prime UTR Variant | AD |
rs13051745 | chr21:41713499 | C>T | SNV | LINC00479 : Intron Variant | ND |
rs16986005 | chr20:41712483 | G>A | SNV | Intergenic | AD |
rs2746177 | chr6:41671837 | G>A | SNV | Intergenic | AD |
rs2746178 | chr6:41671556 | G>C | SNV | Intergenic | AD |
rs2746183 | chr6:41657691 | A>C / A>T | SNV | Intergenic | AD |
rs7981912 | chr13:41622807 | G>A | SNV | VWA8 : Intron Variant | AD |
rs16975393 | chr19:41600012 | C>A | SNV | LOC105372404 : Non Coding Transcript Variant | AD |
rs7556950 | chr2:41582921 | T>C | SNV | Intergenic | AD |
rs7819949 | chr8:41530402 | C>T | SNV | GINS4 : Intron Variant | AD |
rs6809441 | chr3:41453114 | T>C | SNV | ULK4 : Intron Variant | AD |
rs7765789 | chr6:41452404 | A>C | SNV | Intergenic | AD |
rs10446425 | chr3:41443340 | C>A | SNV | ULK4 : Intron Variant | AD | ND |
rs758342 | chr21:41418414 | T>C | SNV | MX1 : 2KB Upstream Variant | AD |
rs7245323 | chr18:41385560 | T>C | SNV | Intergenic | AD |
rs10785246 | chr12:41353626 | C>T | SNV | PDZRN4 : Intron Variant | ND |
rs6929418 | chr6:41339856 | A>G | SNV | NCR2 : Intron Variant | AD |
rs1897224 | chr14:41332026 | T>G | SNV | Intergenic | ND |
rs4890712 | chr18:41323543 | C>A | SNV | Intergenic | AD |
rs7153633 | chr14:41321464 | T>A / T>C | SNV | Intergenic | ND |
rs7160688 | chr14:41316976 | T>A | SNV | Intergenic | ND |
rs1431031 | chr14:41315498 | T>C | SNV | Intergenic | ND |
rs11157219 | chr14:41313498 | A>G | SNV | Intergenic | ND |
rs1453048 | chr4:41304991 | C>T | SNV | Intergenic | AD |
rs11157218 | chr14:41304577 | A>G / A>T | SNV | Intergenic | ND |
rs2798983 | chr14:41303030 | C>T | SNV | Intergenic | ND |
rs2802067 | chr14:41301320 | G>A | SNV | Intergenic | ND |
rs1778369 | chr14:41299542 | T>G | SNV | Intergenic | ND |
rs1431041 | chr14:41297803 | C>T | SNV | Intergenic | ND |
rs1778365 | chr14:41297358 | A>G | SNV | Intergenic | ND |
rs1652920 | chr14:41297081 | T>A | SNV | Intergenic | ND |
rs1782163 | chr14:41296726 | C>T | SNV | Intergenic | ND |
rs1782159 | chr14:41287366 | C>T | SNV | Intergenic | ND |
rs2799787 | chr14:41285347 | G>A | SNV | Intergenic | ND |
rs1782156 | chr14:41283466 | T>A | SNV | Intergenic | ND |
rs1782155 | chr14:41282395 | G>A | SNV | Intergenic | ND |
rs1441231 | chr2:41278333 | T>C | SNV | Intergenic | AD |
rs1778408 | chr14:41274991 | T>C | SNV | Intergenic | ND |
rs1612945 | chr14:41266738 | C>T | SNV | Intergenic | ND |
rs1779517 | chr14:41261318 | C>A / C>G | SNV | Intergenic | ND |
rs1782145 | chr14:41261173 | C>T | SNV | Intergenic | ND |
rs1782144 | chr14:41260570 | G>A | SNV | Intergenic | ND |
rs17027360 | chr2:41259414 | A>G | SNV | Intergenic | AD |
rs1782141 | chr14:41256968 | A>G | SNV | Intergenic | ND |
rs6129784 | chr20:41256889 | T>C | SNV | ZHX3 : Intron Variant | ND |
rs1782139 | chr14:41254382 | A>G | SNV | Intergenic | ND |
rs4861386 | chr4:41252937 | A>C | SNV | UCHL1-AS1 : Intron Variant | CD |
rs7693827 | chr4:41252845 | T>C | SNV | UCHL1-AS1 : Intron Variant | CD |
rs1778401 | chr14:41252558 | A>G | SNV | Intergenic | ND |
rs1779521 | chr14:41251855 | T>C | SNV | Intergenic | ND |
rs1778400 | chr14:41250935 | T>A | SNV | Intergenic | ND |
rs1778399 | chr14:41250163 | G>A | SNV | Intergenic | ND |
rs1782135 | chr14:41246797 | A>G | SNV | Intergenic | ND |
rs1782134 | chr14:41246365 | T>C | SNV | Intergenic | ND |
rs1778392 | chr14:41246301 | G>T | SNV | Intergenic | ND |
rs1611914 | chr14:41233480 | C>T | SNV | Intergenic | ND |
rs1779528 | chr14:41232465 | C>T | SNV | Intergenic | ND |
rs1779530 | chr14:41232115 | C>T | SNV | Intergenic | ND |
rs1779534 | chr14:41230201 | T>C | SNV | Intergenic | ND |
rs1782182 | chr14:41227938 | G>A | SNV | Intergenic | ND |
rs1778379 | chr14:41227751 | A>G | SNV | Intergenic | ND |
rs1782181 | chr14:41227493 | G>A | SNV | Intergenic | ND |
rs1782180 | chr14:41227362 | C>A | SNV | Intergenic | ND |
rs2799789 | chr14:41223783 | A>C | SNV | Intergenic | ND |
rs1782167 | chr14:41204511 | G>A | SNV | Intergenic | ND |
rs6672508 | chr1:41200899 | C>G / C>T | SNV | SCMH1 : Intron Variant | AD |
rs2691678 | chr3:41188832 | A>G | SNV | Intergenic | AD |
rs13266712 | chr8:41126541 | C>A / C>T | SNV | Intergenic | OD |
rs737505 | chr8:41122871 | C>T | SNV | Intergenic | AD |
rs12548368 | chr8:41116048 | A>G | SNV | Intergenic | AD |
rs12547609 | chr8:41114714 | A>C | SNV | Intergenic | AD |
rs12550040 | chr8:41109645 | G>A / G>T | SNV | Intergenic | AD |
rs6474300 | chr8:41108162 | A>G | SNV | Intergenic | AD |
rs1959909 | chr14:41088123 | A>C | SNV | LOC644919 : Intron Variant | ND |
rs1954456 | chr14:41086559 | T>C / T>G | SNV | LOC644919 : Intron Variant | ND |
rs115368721 | chr4:41054822 | G>A | SNV | APBB2 : Intron Variant | OD |
rs114070671 | chr4:41054699 | A>G | SNV | APBB2 : Intron Variant | OD |
rs76617915 | chr19:41032173 | G>A / G>T | SNV | Intergenic | ND |
rs1552223 | chr19:41020047 | G>A | SNV | Intergenic | AD |
rs17357905 | chr1:41018645 | T>C | SNV | SLFNL1 : Intron Variant SLFNL1-AS1 : Intron Variant | AD |
rs2837900 | chr21:41014748 | T>C | SNV | Intergenic | AD |
rs2279343 | chr19:41009358 | A>G | SNV | CYP2B6 : Missense Variant | ND |
rs12889050 | chr14:40971126 | C>T | SNV | LOC644919 : Intron Variant | AD |
rs1176968 | chr14:40964101 | G>A | SNV | LOC644919 : Intron Variant | AD |
rs12890528 | chr14:40935888 | C>A / C>T | SNV | Intergenic | AD |
rs76935404 | chr19:40913389 | C>T | SNV | Intergenic | ND |
rs10425738 | chr19:40911822 | G>A | SNV | Intergenic | ND |
rs73931391 | chr19:40901969 | A>G | SNV | LOC107985299 : Intron Variant | ND |
rs4079366 | chr19:40878770 | T>A / T>C | SNV | CYP2A7 : Missense Variant | ND |
rs7247903 | chr19:40866570 | A>G | SNV | Intergenic | ND |
rs3875150 | chr19:40864271 | T>A / T>C / T>G | SNV | Intergenic | ND |
rs111645190 | chr19:40855903 | G>A | SNV | Intergenic | ND |
rs6102185 | chr20:40849893 | G>A | SNV | Intergenic | ND |
rs56256500 | chr19:40848266 | G>A / G>C / G>T | SNV | CYP2A6 : Missense Variant | ND |
rs56113850 | chr19:40847202 | T>C | SNV | CYP2A6 : Intron Variant | ND |
rs1349568 | chr14:40846740 | A>C | SNV | LOC105370467 : Intron Variant | AD |
rs6029379 | chr20:40844475 | T>C | SNV | Intergenic | ND |
rs704034 | chr5:40842014 | A>G | SNV | CARD6 : Intron Variant | ND |
rs2316205 | chr19:40840863 | T>C | SNV | Intergenic | ND |
rs12459249 | chr19:40833991 | T>C | SNV | Intergenic | ND |
rs11878604 | chr19:40827379 | T>C | SNV | Intergenic | ND |
rs116478358 | chr4:40826202 | T>A | SNV | APBB2 : Intron Variant | CD |
rs111825958 | chr19:40825304 | C>A | SNV | Intergenic | ND |
rs7507400 | chr19:40824274 | G>T | SNV | Intergenic | ND |
rs2545770 | chr19:40818275 | C>A | SNV | Intergenic | ND |
rs185308415 | chr19:40811274 | A>G | SNV | Intergenic | ND |
rs17620991 | chr7:40796922 | G>C / G>T | SNV | SUGCT : Intron Variant | AD |
rs8128946 | chr21:40784506 | A>G | SNV | DSCAM : Intron Variant | AD |
rs2412546 | chr15:40714325 | G>A | SNV | RAD51 : Intron Variant | AD |
rs3092155 | chr20:40413231 | A>G | SNV | Intergenic | ND |
rs6755144 | chr2:40409100 | A>G | SNV | SLC8A1 : Intron Variant | AD |
rs9789765 | chr2:40407694 | A>T | SNV | SLC8A1 : Intron Variant | AD |
rs10490045 | chr2:40404215 | T>C | SNV | SLC8A1 : Intron Variant | AD |
rs10490046 | chr2:40403538 | A>C | SNV | SLC8A1 : Intron Variant | AD |
rs2436728 | chr6:40397862 | G>A | SNV | LRFN2 : Intron Variant | AD |
rs7247916 | chr19:40310623 | A>G | SNV | C19orf47 : Intron Variant | AD |
rs2925009 | chr8:40280820 | C>G | SNV | Intergenic | AD |
rs10501226 | chr11:40280456 | T>C | SNV | LRRC4C : Intron Variant | AD |
rs2837524 | chr21:40233218 | C>T | SNV | DSCAM : Intron Variant | ND |
rs4369393 | chr11:40204831 | G>T | SNV | LRRC4C : Intron Variant | AD |
rs12074893 | chr1:40162447 | C>T | SNV | RLF : Intron Variant LOC105378671 : 2KB Upstream Variant | AD |
rs6600318 | chr1:40135964 | T>C | SNV | Intergenic | AD |
rs2548145 | chr5:40134675 | G>A | SNV | Intergenic | AD |
rs2837437 | chr21:40126099 | T>C | SNV | DSCAM : Intron Variant | AD |
rs16999304 | chr21:40119439 | T>C | SNV | DSCAM : Intron Variant | AD |
rs6688203 | chr1:40084258 | C>A | SNV | PPT1 : Intron Variant | AD |
rs16934315 | chr11:40071243 | T>C | SNV | Intergenic | AD |
rs2837420 | chr21:40070721 | A>G | SNV | DSCAM : Intron Variant | ND |
rs16826852 | chr1:40065422 | A>G | SNV | CAP1 : Intron Variant | AD |
rs10768576 | chr11:40052270 | G>A / G>C | SNV | Intergenic | AD |
rs12402428 | chr1:40038053 | T>C | SNV | LOC105378669 : Intron Variant | AD |
rs6485172 | chr11:40019740 | A>G | SNV | Intergenic | AD |
rs7111117 | chr11:39968412 | T>C | SNV | Intergenic | AD |
rs3131706 | chr1:39947426 | T>C | SNV | Intergenic | ND |
rs1598994 | chr3:39934271 | T>G | SNV | MYRIP : Intron Variant | ND |
rs2837302 | chr21:39931970 | C>A / C>T | SNV | Intergenic | AD |
rs7276341 | chr21:39915132 | A>G | SNV | PCP4 : Intron Variant | AD |
rs1599903 | chr3:39913575 | A>C | SNV | MYRIP : Intron Variant | ND |
rs10837301 | chr11:39912418 | A>C | SNV | LOC105376637 : Intron Variant | AD |
rs7135349 | chr12:39890752 | C>T | SNV | C12orf40 : Intron Variant SLC2A13 : Intron Variant | ND |
rs10768556 | chr11:39880893 | C>A | SNV | LOC105376637 : Intron Variant | AD |
rs7566309 | chr2:39869258 | A>G | SNV | Intergenic | AD |
rs616650 | chr19:39837975 | C>T | SNV | FBL : Intron Variant | AD |
rs17718330 | chr15:39831148 | T>C | SNV | GPR176 : Intron Variant | AD |
rs1972537 | chr19:39765688 | G>A | SNV | Intergenic | AD |
rs79978308 | chr21:39648618 | C>G / C>T | SNV | B3GALT5 : Intron Variant | AD |
rs1026526 | chr6:39619981 | A>G | SNV | KIF6 : Intron Variant | AD |
rs9394619 | chr6:39606601 | T>C | SNV | KIF6 : Intron Variant | AD |
rs1619021 | chr17:39583021 | G>A | SNV | Intergenic | AD |
rs4794814 | chr17:39540599 | G>A | SNV | CDK12 : Intron Variant | AD |
rs6901155 | chr6:39532803 | C>A | SNV | KIF6 : Intron Variant | ND |
rs7503705 | chr17:39513451 | A>G | SNV | CDK12 : Intron Variant | AD |
rs11657899 | chr17:39470710 | G>A | SNV | CDK12 : Intron Variant | AD |
rs4236064 | chr6:39446251 | G>T | SNV | KIF6 : Intron Variant | AD |
rs7317775 | chr13:39440781 | T>A | SNV | LHFP : Intron Variant | AD |
rs9594332 | chr13:39434823 | G>A | SNV | LHFP : Intron Variant | AD |
rs7501488 | chr17:39420164 | T>G | SNV | MED1 : Intron Variant | AD |
rs12452509 | chr17:39418469 | G>A | SNV | MED1 : Intron Variant | AD |
rs6503513 | chr17:39405360 | A>G | SNV | MED1 : Intron Variant | AD |
rs4810264 | chr20:39391934 | C>G | SNV | Intergenic | ND |
rs13341996 | chr17:39380609 | C>T | SNV | FBXL20 : Intron Variant | AD |
rs4511574 | chr17:39376663 | C>T | SNV | FBXL20 : Intron Variant | AD |
rs4821888 | chr22:39374592 | A>G / A>T | SNV | SYNGR1 : Intron Variant | AD |
rs1569499 | chr22:39373813 | T>C | SNV | SYNGR1 : Intron Variant | AD |
rs5757642 | chr22:39368819 | T>C | SNV | SYNGR1 : Intron Variant | AD |
rs30454 | chr19:39353536 | G>A | SNV | SAMD4B : Intron Variant | AD |
rs8069451 | chr17:39348680 | T>C | SNV | FBXL20 : Intron Variant | AD |
rs2067008 | chr20:39336456 | G>A / G>T | SNV | Intergenic | ND |
rs3786949 | chr19:39335839 | G>A | SNV | GMFG : Intron Variant | AD |
rs7220650 | chr17:39330915 | T>C | SNV | FBXL20 : Intron Variant | AD |
rs7181250 | chr15:39330392 | T>C | SNV | LOC105370777 : Intron Variant | AD |
rs30461 | chr19:39298475 | A>G | SNV | IFNL1 : Missense Variant | AD |
rs585961 | chr17:39287783 | G>A | SNV | FBXL20 : Intron Variant | AD |
rs7830120 | chr8:39274171 | G>A | SNV | ADAM32 : Intron Variant | AD |
rs7700754 | chr5:39252920 | G>A | SNV | FYB : Intron Variant | ND |
rs883544 | chr17:39231160 | A>G | SNV | Intergenic | AD |
rs6028335 | chr20:39216834 | A>G | SNV | LOC107985448 : Intron Variant LOC339568 : Intron Variant | ND |
rs696748 | chr5:39213594 | A>G | SNV | FYB : Intron Variant | ND |
rs5750769 | chr22:39196176 | C>T | SNV | Intergenic | AD |
rs41437948 | chr7:39159265 | T>G | SNV | POU6F2 : Intron Variant | AD |
rs2242930 | chr21:39029033 | G>A | SNV | LOC107985484 : Non Coding Transcript Variant | AD |
rs2836823 | chr21:39008323 | C>T | SNV | LOC102724740 : Intron Variant | ND |
rs2836800 | chr21:38975759 | C>T | SNV | LOC101928435 : Non Coding Transcript Variant | AD |
rs4974983 | chr4:38969437 | A>G | SNV | TMEM156 : Intron Variant | AD |
rs2094081 | chr1:38927359 | G>A / G>C | SNV | RHBDL2 : Intron Variant | AD |
rs10392 | chr20:38922292 | G>A | SNV | PPP1R16B : 3 Prime UTR Variant | AD |
rs4714198 | chr6:38909829 | C>A | SNV | DNAH8 : Intron Variant LOC100131047 : Intron Variant | AD |
rs82977 | chr17:38908095 | G>A | SNV | LASP1 : Intron Variant | ND |
rs11943027 | chr4:38880267 | G>C | SNV | FAM114A1 : Intron Variant | AD |
rs1320454 | chr1:38825472 | C>A / C>T | SNV | Intergenic | AD |
rs7288826 | chr22:38818769 | G>T | SNV | NPTXR : 3 Prime UTR Variant | ND |
rs17616434 | chr4:38811255 | T>C | SNV | Intergenic | AD |
rs5743604 | chr4:38799664 | A>G | SNV | TLR1 : Intron Variant | AD |
rs4373300 | chr5:38798647 | G>A | SNV | OSMR-AS1 : Intron Variant | AD |
rs4833095 | chr4:38798089 | T>C | SNV | TLR1 : Missense Variant | AD |
rs7706715 | chr5:38792384 | C>A / C>G | SNV | OSMR-AS1 : Intron Variant LOC107986414 : Non Coding Transcript Variant | AD |
rs4543123 | chr4:38790903 | A>G | SNV | TLR1 : Non Coding Transcript Variant | AD |
rs6531663 | chr4:38790719 | T>C | SNV | TLR1 : Non Coding Transcript Variant | AD |
rs4833093 | chr4:38788119 | G>T | SNV | TLR1 : Non Coding Transcript Variant | AD |
rs6834581 | chr4:38786613 | T>C | SNV | Intergenic | AD |
rs1056104 | chr2:38781807 | G>A / G>C | SNV | GEMIN6 : Missense Variant | ND |
rs35795311 | chr15:38706468 | C>G | SNV | Intergenic | AD |
rs36094159 | chr15:38706194 | G>A | SNV | Intergenic | AD |
rs7183893 | chr15:38704780 | A>C | SNV | Intergenic | AD |
rs12899449 | chr15:38703290 | A>G | SNV | Intergenic | AD |
rs12901215 | chr15:38700692 | G>A | SNV | Intergenic | AD |
rs2132157 | chr15:38700346 | A>G | SNV | C15orf53 : 500B Downstream Variant | AD |
rs12916379 | chr15:38699319 | A>G | SNV | C15orf53 : 3 Prime UTR Variant | AD |
rs2172835 | chr15:38697970 | C>T | SNV | C15orf53 : Intron Variant | AD |
rs35024396 | chr15:38697569 | G>A | SNV | C15orf53 : Intron Variant | AD |
rs34281605 | chr15:38697473 | G>A | SNV | C15orf53 : Intron Variant | AD |
rs34141940 | chr15:38697456 | G>A | SNV | C15orf53 : Intron Variant | AD |
rs34356257 | chr15:38697404 | T>A / T>C | SNV | C15orf53 : Intron Variant | AD |
rs7165988 | chr15:38696614 | C>G / C>T | SNV | C15orf53 : Missense Variant | AD |
rs7171233 | chr15:38696559 | T>A | SNV | C15orf53 : 2KB Upstream Variant | AD |
rs7163869 | chr15:38696190 | G>C | SNV | C15orf53 : 2KB Upstream Variant | AD |
rs35102843 | chr15:38695906 | C>A | SNV | C15orf53 : 2KB Upstream Variant | AD |
rs12903120 | chr15:38695896 | G>T | SNV | C15orf53 : 2KB Upstream Variant | AD |
rs12898460 | chr15:38694612 | C>T | SNV | C15orf53 : 2KB Upstream Variant | AD |
rs12912251 | chr15:38694167 | G>T | SNV | Intergenic | AD |
rs1874252 | chr15:38670555 | G>T | SNV | LOC105370775 : 2KB Upstream Variant | AD |
rs7168475 | chr15:38668681 | A>C / A>G | SNV | Intergenic | AD |
rs2814889 | chr6:38551985 | C>T | SNV | BTBD9 : Intron Variant | AD |
rs1004064 | chr4:38456999 | G>A | SNV | LINC01258 : Intron Variant | AD |
rs12997019 | chr2:38455577 | T>C | SNV | Intergenic | AD |
rs7328507 | chr13:38448054 | T>C | SNV | Intergenic | ND |
rs932026 | chr18:38425547 | G>A | SNV | Intergenic | AD |
rs2836364 | chr21:38395952 | C>T | SNV | ERG : Intron Variant | AD |
rs6847801 | chr4:38296648 | C>G / C>T | SNV | Intergenic | ND |
rs1543632 | chr1:38282288 | C>T | SNV | Intergenic | AD |
rs6969314 | chr7:38136771 | G>A | SNV | Intergenic | AD |
rs16937688 | chr10:38127545 | C>T | SNV | ZNF37A : Intron Variant | AD |
rs10502685 | chr18:38098747 | C>A | SNV | Intergenic | AD |
rs17536346 | chr18:38087951 | A>G | SNV | Intergenic | AD |
rs11211383 | chr1:38016684 | T>G | SNV | UTP11 : Intron Variant | AD |
rs6901928 | chr6:37969526 | T>C | SNV | ZFAND3 : Intron Variant | AD |
rs16994074 | chr4:37924357 | T>C | SNV | TBC1D1 : Intron Variant LOC105374407 : 2KB Upstream Variant | CD |
rs2216712 | chr5:37918601 | C>T | SNV | LOC105374728 : Non Coding Transcript Variant | AD |
rs11717973 | chr3:37720523 | C>T | SNV | ITGA9 : Intron Variant | ND |
rs531454 | chr1:37707925 | A>G | SNV | CDCA8 : Intron Variant | AD |
rs615530 | chr1:37696022 | A>G | SNV | CDCA8 : Intron Variant | AD |
rs1982389 | chr7:37687349 | A>G | SNV | GPR141 : Intron Variant | AD |
rs2835872 | chr21:37654970 | G>A | SNV | KCNJ6 : Intron Variant | AD |
rs3761442 | chr22:37607063 | C>T | SNV | GGA1 : 2KB Upstream Variant | AD |
rs6458004 | chr6:37594927 | T>C | SNV | Intergenic | AD |
rs11621659 | chr14:37578238 | G>A | SNV | MIPOL1 : Intron Variant | ND |
rs4821670 | chr22:37574859 | T>C | SNV | LGALS2 : Intron Variant | AD |
rs6550481 | chr3:37573219 | T>A / T>G | SNV | ITGA9 : Intron Variant | ND |
rs981794 | chr14:37571550 | A>G | SNV | MIPOL1 : Intron Variant | ND |
rs919113 | chr3:37558979 | A>G | SNV | ITGA9 : Intron Variant | ND |
rs11969056 | chr6:37516509 | C>T | SNV | LOC100505530 : Intron Variant | ND |
rs10502674 | chr18:37507420 | C>T | SNV | CELF4 : Intron Variant | AD |
rs2646937 | chr6:37501761 | C>T | SNV | CCDC167 : 2KB Upstream Variant | AD |
rs28887513 | chr15:37479865 | A>C / A>G | SNV | Intergenic | CD |
rs2835725 | chr21:37418854 | A>G | SNV | DYRK1A : Intron Variant | AD |
rs66691212 | chr11:37364436 | T>G | SNV | Intergenic | CD |
rs6940938 | chr6:37340818 | G>C | SNV | LOC105375040 : Intron Variant | ND |
rs195411 | chr6:37333341 | A>G | SNV | TBC1D22B : 500B Downstream Variant | AD |
rs11895771 | chr2:37185792 | T>G | SNV | SULT6B1 : Intron Variant | AD |
rs2395670 | chr6:37115033 | A>G | SNV | Intergenic | ND |
rs9985748 | chr4:37083087 | G>A / G>T | SNV | LOC101928721 : Intron Variant | AD |
rs10484210 | chr4:37074374 | A>C / A>G | SNV | LOC101928721 : Intron Variant | AD |
rs28797478 | chrX:37016604 | G>A | SNV | Intergenic | AD |
rs708006 | chr6:36966468 | C>A | SNV | Intergenic | AD |
rs837136 | chr15:36920696 | G>A | SNV | MEIS2 : Intron Variant | AD |
rs3824339 | chr9:36885749 | G>A / G>T | SNV | PAX5 : Intron Variant | AD |
rs576434 | chr13:36884002 | T>C | SNV | SMAD9 : Intron Variant | AD |
rs75913810 | chr6:36800584 | G>A | SNV | CPNE5 : Intron Variant | AD |
rs7322307 | chr13:36776542 | A>G | SNV | LOC102723490 : Intron Variant | AD |
rs3897230 | chr13:36773840 | C>T | SNV | LOC102723490 : Intron Variant | AD |
rs7769970 | chr6:36767703 | C>G / C>T | SNV | CPNE5 : Intron Variant | AD |
rs826969 | chr19:36756570 | G>T | SNV | ZNF850 : Intron Variant | ND |
rs4756348 | chr11:36755789 | T>G | SNV | LOC107984326 : Intron Variant | AD |
rs10116484 | chr9:36741030 | C>T | SNV | Intergenic | AD |
rs7873864 | chr9:36740960 | G>A | SNV | Intergenic | AD |
rs7857754 | chr9:36738644 | G>A / G>C | SNV | Intergenic | AD |
rs9977521 | chr21:36710512 | C>T | SNV | SIM2 : Intron Variant | AD |
rs7685223 | chr4:36660237 | G>A | SNV | Intergenic | CD |
rs6959295 | chr7:36659079 | C>T | SNV | AOAH : Intron Variant | CD |
rs1321311 | chr6:36655123 | C>A | SNV | Intergenic | AD |
rs1321313 | chr6:36651044 | C>T | SNV | Intergenic | AD |
rs2246564 | chr9:36638248 | A>T | SNV | MELK : Intron Variant | AD |
rs6000351 | chr22:36614820 | G>A | SNV | CACNG2 : Intron Variant | ND |
rs10972978 | chr9:36576850 | A>G | SNV | MELK : Intron Variant | AD |
rs11033637 | chr11:36458239 | G>A | SNV | PRR5L : Intron Variant | AD |
rs878913 | chr18:36454768 | C>G / C>T | SNV | FHOD3 : Intron Variant | CD |
rs2292648 | chr11:36425819 | A>G | SNV | PRR5L : Intron Variant | AD |
rs16822823 | chr1:36408641 | A>G | SNV | Intergenic | AD |
rs4451521 | chr1:36365663 | C>G | SNV | STK40 : Intron Variant | AD |
rs11583322 | chr1:36356711 | T>C | SNV | STK40 : Intron Variant | AD |
rs10490672 | chr2:36343996 | A>C | SNV | Intergenic | AD |
rs12418187 | chr11:36334692 | C>T | SNV | PRR5L : Intron Variant | AD |
rs12116935 | chr1:36323945 | A>G | SNV | SH3D21 : Intron Variant EVA1B : 5 Prime UTR Variant | AD |
rs670603 | chr8:36301253 | C>T | SNV | Intergenic | AD |
rs7044830 | chr9:36293160 | C>T | SNV | LOC102724322 : Non Coding Transcript Variant | AD |
rs2284642 | chr21:36279015 | G>T | SNV | DOPEY2 : Intron Variant | AD |
rs16962759 | chr15:36256687 | T>C | SNV | Intergenic | AD |
rs35852281 | chr15:36228793 | C>T | SNV | Intergenic | AD |
rs522468 | chr1:36188076 | T>G | SNV | Intergenic | AD |
rs6563354 | chr13:36122357 | C>T | SNV | DCLK1 : Intron Variant | AD |
rs11033401 | chr11:36073797 | G>A | SNV | LDLRAD3 : Intron Variant LOC101928510 : Intron Variant | AD |
rs7982504 | chr13:36067886 | T>A | SNV | DCLK1 : Intron Variant | ND |
rs1882051 | chr7:36064656 | T>A / T>C | SNV | Intergenic | AD |
rs10215376 | chr7:36038205 | C>T | SNV | Intergenic | ND |
rs1873117 | chr2:36036324 | T>C | SNV | Intergenic | ND |
rs10511924 | chr9:36007608 | G>C | SNV | Intergenic | ND |
rs9545925 | chr13:35961055 | G>T | SNV | DCLK1 : Intron Variant | AD |
rs2949081 | chr2:35944468 | T>G | SNV | Intergenic | AD |
rs2968625 | chr2:35938765 | G>A | SNV | Intergenic | AD |
rs1714081 | chr4:35936553 | C>T | SNV | Intergenic | ND |
rs5999984 | chr22:35724463 | G>C | SNV | APOL5 : Intron Variant | AD |
rs12972040 | chr19:35577160 | G>C | SNV | Intergenic | AD |
rs11096778 | chr4:35567288 | T>C | SNV | Intergenic | ND |
rs1425465 | chr4:35558018 | A>G | SNV | Intergenic | ND |
rs6836555 | chr4:35556858 | C>T | SNV | Intergenic | ND |
rs11942729 | chr4:35554744 | T>C | SNV | Intergenic | ND |
rs10517352 | chr4:35552967 | T>G | SNV | Intergenic | ND |
rs6531380 | chr4:35529029 | C>T | SNV | Intergenic | ND |
rs4301139 | chr4:35522896 | T>G | SNV | Intergenic | ND |
rs4349619 | chr4:35522461 | T>A | SNV | Intergenic | ND |
rs4498148 | chr4:35522299 | C>T | SNV | Intergenic | ND |
rs4859365 | chr4:35520910 | G>A | SNV | Intergenic | ND |
rs4859306 | chr4:35520575 | A>C / A>G | SNV | Intergenic | ND |
rs4859305 | chr4:35520415 | T>C | SNV | Intergenic | ND |
rs5002773 | chr4:35518928 | C>G | SNV | Intergenic | ND |
rs5002776 | chr4:35518855 | A>T | SNV | Intergenic | ND |
rs7664882 | chr4:35517734 | T>A | SNV | Intergenic | ND |
rs6814075 | chr4:35516255 | T>C | SNV | Intergenic | ND |
rs2375489 | chr4:35515534 | T>C | SNV | Intergenic | ND |
rs4566673 | chr4:35515173 | A>C | SNV | Intergenic | ND |
rs6531367 | chr4:35514005 | A>G | SNV | Intergenic | ND |
rs6531366 | chr4:35513892 | A>C / A>G | SNV | Intergenic | ND |
rs6531365 | chr4:35513859 | A>C | SNV | Intergenic | ND |
rs7659440 | chr4:35513788 | G>T | SNV | Intergenic | ND |
rs4613591 | chr4:35511728 | A>C / A>T | SNV | Intergenic | ND |
rs7332116 | chr13:35504290 | C>A | SNV | NBEA : Intron Variant | ND |
rs907978 | chr4:35487287 | A>G | SNV | Intergenic | ND |
rs6827035 | chr4:35473477 | G>A / G>C | SNV | Intergenic | ND |
rs1113371 | chr4:35460417 | A>C | SNV | Intergenic | ND |
rs960740 | chr4:35457552 | T>A / T>G | SNV | Intergenic | ND |
rs317045 | chr4:35434119 | G>A | SNV | Intergenic | ND |
rs317047 | chr4:35433088 | A>G | SNV | Intergenic | ND |
rs1004584 | chr7:35430618 | C>T | SNV | Intergenic | AD |
rs317028 | chr4:35423761 | C>T | SNV | Intergenic | ND |
rs317031 | chr4:35421494 | C>A / C>G | SNV | Intergenic | ND |
rs317026 | chr4:35412125 | T>C | SNV | Intergenic | ND |
rs13235830 | chr7:35411290 | G>T | SNV | Intergenic | AD |
rs13234350 | chr7:35406974 | T>C | SNV | Intergenic | AD |
rs7152826 | chr14:35393198 | C>A | SNV | Intergenic | AD |
rs11666282 | chr19:35316942 | C>T | SNV | Intergenic | AD |
rs899940 | chr17:35259821 | T>G | SNV | SLFN5 : Intron Variant | AD |
rs9908966 | chr17:35256583 | G>A | SNV | SLFN5 : Intron Variant | AD |
rs2092029 | chr22:35256248 | C>T | SNV | HMGXB4 : 2KB Upstream Variant LOC105373017 : Intron Variant | AD |
rs17629798 | chr17:35219913 | T>C | SNV | Intergenic | ND |
rs4610908 | chrX:35166418 | G>A | SNV | Intergenic | AD | ND |
rs1415771 | chr20:35146690 | G>A | SNV | EDEM2 : Intron Variant | AD |
rs17629188 | chr17:35130009 | G>A / G>T | SNV | FNDC8 : Intron VariantNLE1 : 3 Prime UTR Variant | AD |
rs9622147 | chr22:35107079 | C>T | SNV | Intergenic | AD |
rs16960370 | chr15:35103523 | A>G | SNV | LOC105370765 : 2KB Upstream Variant | AD |
rs7228414 | chr18:35054670 | A>G | SNV | MAPRE2 : Intron Variant | AD |
rs40200 | chr5:35045640 | A>G | SNV | AGXT2 : Intron Variant | ND |
rs3736802 | chr20:35016239 | T>C | SNV | TRPC4AP : Intron Variant | AD |
rs17398711 | chr2:35010053 | C>A / C>T | SNV | Intergenic | AD |
rs2140418 | chr6:35007638 | T>C | SNV | ANKS1A : Intron Variant | AD |
rs7282535 | chr21:35004924 | A>T | SNV | RUNX1 : Intron Variant | ND |
rs17387182 | chr2:34999384 | C>T | SNV | LOC105374461 : Intron Variant | AD |
rs6579204 | chr20:34965874 | A>G | SNV | MYH7B : Intron Variant | AD |
rs6088664 | chr20:34963297 | G>A | SNV | MYH7B : Intron Variant | AD |
rs6060124 | chr20:34949094 | C>A | SNV | GSS : Intron Variant | AD |
rs77109747 | chr1:34947470 | G>A | SNV | Intergenic | ND |
rs847848 | chr6:34938391 | T>C | SNV | ANKS1A : Intron Variant | AD |
rs847851 | chr6:34936807 | G>A | SNV | ANKS1A : Intron Variant | AD |
rs1737727 | chr6:34936711 | T>C | SNV | ANKS1A : Intron Variant | AD |
rs2273006 | chr6:34883357 | T>C / T>G | SNV | TAF11 : Intron Variant | AD |
rs2834649 | chr21:34837353 | G>A | SNV | RUNX1 : Intron Variant LOC102724584 : Intron Variant | ND |
rs2253319 | chr21:34815749 | C>T | SNV | RUNX1 : Intron Variant | ND |
rs137270 | chr22:34771592 | G>A | SNV | Intergenic | ND |
rs6060038 | chr20:34769912 | G>A | SNV | NCOA6 : Intron Variant | AD |
rs6141509 | chr20:34731584 | G>A | SNV | NCOA6 : Intron Variant | AD |
rs16970282 | chr17:34705079 | A>C | SNV | Intergenic | AD |
rs7936502 | chr11:34638260 | G>T | SNV | EHF : Intron Variant | AD |
rs988199 | chr17:34556237 | G>A | SNV | Intergenic | AD |
rs758411 | chr17:34549927 | A>G | SNV | Intergenic | AD |
rs4821261 | chr22:34545584 | T>C | SNV | Intergenic | AD |
rs6088519 | chr20:34544387 | C>T | SNV | Intergenic | AD |
rs990510 | chr17:34542932 | C>A | SNV | Intergenic | AD |
rs1860275 | chr17:34533630 | G>A | SNV | Intergenic | AD |
rs4713806 | chr6:34506852 | C>T | SNV | PACSIN1 : Intron Variant | AD |
rs5927282 | chrX:34501959 | C>T | SNV | Intergenic | ND |
rs16930094 | chr11:34500102 | C>T | SNV | ELF5 : Intron Variant | ND |
rs4713797 | chr6:34490756 | A>G | SNV | PACSIN1 : Intron Variant | AD |
rs10941189 | chr5:34489443 | C>A | SNV | Intergenic | AD |
rs12273124 | chr11:34458164 | A>G | SNV | CAT : Intron Variant | AD |
rs12269988 | chr11:34451227 | A>G | SNV | CAT : Intron Variant | AD |
rs11032702 | chr11:34446576 | C>T | SNV | CAT : Intron Variant | AD |
rs10753308 | chr1:34441547 | A>G | SNV | Intergenic | ND |
rs12272630 | chr11:34440118 | G>C | SNV | CAT : Intron Variant | AD |
rs1107573 | chr11:34434661 | C>T | SNV | LOC105376622 : Intron Variant | AD |
rs12295136 | chr11:34428914 | T>C | SNV | Intergenic | AD |
rs16925514 | chr11:34427713 | G>T | SNV | Intergenic | AD |
rs17031657 | chr3:34405246 | A>C | SNV | LOC101928114 : Intron Variant | AD |
rs1529075 | chr3:34386453 | T>G | SNV | LOC101928114 : Intron Variant | AD |
rs1362182 | chr7:34335941 | G>A | SNV | Intergenic | AD |
rs7105914 | chr11:34245136 | T>C | SNV | ABTB2 : Intron Variant | AD |
rs2473918 | chr11:34169406 | T>C | SNV | ABTB2 : Intron Variant | ND |
rs745809 | chr11:34166300 | G>A | SNV | ABTB2 : Intron Variant | AD |
rs5928439 | chrX:34162711 | A>G | SNV | Intergenic | AD |
rs11639310 | chr15:34129750 | C>T | SNV | Intergenic | AD |
rs3006120 | chrX:34119210 | G>A | SNV | Intergenic | AD |
rs1362456 | chr7:34064613 | G>A | SNV | BMPER : Intron Variant | AD |
rs2625684 | chr1:34039514 | T>C | SNV | CSMD2 : Intron Variant | AD |
rs2164581 | chr1:34025957 | A>G | SNV | CSMD2 : Intron Variant | AD |
rs2358756 | chr1:34014321 | T>C | SNV | CSMD2 : Intron Variant | AD |
rs11129574 | chr3:33972800 | C>T | SNV | Intergenic | AD |
rs7620363 | chr3:33971713 | C>T | SNV | Intergenic | AD | ND |
rs35405 | chr5:33945653 | C>T | SNV | SLC45A2 : Intron Variant | ND |
rs9380389 | chr6:33935299 | A>G | SNV | Intergenic | AD |
rs7536114 | chr1:33913774 | T>G | SNV | CSMD2 : Intron Variant | AD |
rs911216 | chr1:33909598 | A>C | SNV | CSMD2 : Intron Variant | AD |
rs2213360 | chr22:33895762 | A>G | SNV | LARGE : Intron Variant | AD |
rs6120401 | chr20:33879333 | C>T | SNV | Intergenic | AD |
rs7172406 | chr15:33849304 | G>T | SNV | RYR3 : Intron Variant | ND |
rs5999108 | chr22:33805813 | T>C | SNV | LARGE : Intron Variant | AD |
rs17231134 | chr10:33790045 | G>A / G>T | SNV | Intergenic | AD |
rs2296744 | chr6:33772605 | G>A | SNV | LEMD2 : 3 Prime UTR Variant | ND |
rs4287749 | chr2:33744320 | G>A | SNV | LINC01317 : Intron Variant | AD |
rs7533254 | chr1:33716230 | G>A | SNV | CSMD2 : Intron Variant | AD |
rs2746600 | chr11:33693095 | A>G | SNV | LOC105376617 : Intron Variant | AD |
rs831620 | chr11:33687727 | A>G | SNV | LOC105376617 : Intron Variant | AD |
rs5754638 | chr22:33682071 | A>G / A>T | SNV | LARGE : Intron Variant | AD |
rs9876025 | chr3:33656680 | G>A | SNV | CLASP2 : Intron Variant | AD |
rs1565937 | chr15:33603990 | C>T | SNV | RYR3 : Intron Variant | AD |
rs16973062 | chr15:33600096 | T>C | SNV | RYR3 : Intron Variant | AD |
rs7293114 | chr22:33589329 | A>G | SNV | LARGE : Intron Variant | AD |
rs416391 | chr1:33582668 | C>T | SNV | CSMD2 : Intron Variant | AD |
rs6701268 | chr1:33575591 | T>G | SNV | CSMD2 : Intron Variant | AD |
rs4144333 | chr15:33502351 | A>G | SNV | RYR3 : Intron Variant | AD |
rs7561821 | chr2:33490675 | T>G | SNV | RASGRP3 : Intron Variant | AD |
rs10798953 | chr1:33471534 | T>C | SNV | ZSCAN20 : 2KB Upstream Variant | AD |
rs6827883 | chr4:33442785 | C>T | SNV | Intergenic | AD |
rs2676029 | chr15:33430601 | C>T | SNV | RYR3 : Intron Variant | ND |
rs2036535 | chr17:33423995 | G>A | SNV | ASIC2 : Intron Variant | ND |
rs5998935 | chr22:33411849 | G>A / G>C | SNV | LARGE : Intron Variant | ND |
rs17571355 | chr14:33400670 | A>C | SNV | NPAS3 : Intron Variant | AD |
rs17101003 | chr14:33399174 | G>A | SNV | NPAS3 : Intron Variant | AD |
rs17236010 | chr15:33396486 | C>T | SNV | RYR3 : Intron Variant | AD |
rs12291056 | chr11:33393605 | G>A | SNV | KIAA1549L : Intron Variant | AD |
rs17251987 | chr9:33388291 | C>T | SNV | AQP7 : Intron Variant | AD |
rs871355 | chr8:33357908 | C>T | SNV | FUT10 : Intron Variant | CD |
rs11722181 | chr4:33353324 | A>C | SNV | Intergenic | AD |
rs2243668 | chr10:33274965 | G>A | SNV | NRP1 : Intron Variant | AD |
rs7653239 | chr3:33248104 | G>A | SNV | Intergenic | AD |
rs4389431 | chr3:33201894 | C>T | SNV | SUSD5 : Intron Variant | AD |
rs17667691 | chr18:33198122 | G>A | SNV | CCDC178 : Intron Variant | ND |
rs7218135 | chr17:33166325 | G>T | SNV | ASIC2 : Intron Variant | ND |
rs676069 | chr1:33156476 | T>C | SNV | AZIN2 : Intron Variant TRIM62 : Intron Variant | AD |
rs10432656 | chr2:33149965 | C>T | SNV | LTBP1 : Intron Variant | ND |
rs78109725 | chr20:33108365 | C>A | SNV | BPIFB4 : Intron Variant | CD |
rs642899 | chr13:33106717 | T>G | SNV | STARD13 : Intron Variant | AD |
rs6120085 | chr20:33010975 | T>C | SNV | BPIFB2 : Intron Variant | AD |
rs10483422 | chr14:33009299 | A>G | SNV | NPAS3 : Intron Variant | ND |
rs983579 | chr12:32991864 | G>A / G>C | SNV | Intergenic | ND |
rs12586198 | chr14:32972410 | T>C | SNV | NPAS3 : Intron Variant | ND |
rs17739703 | chr18:32943324 | T>C | SNV | CCDC178 : Intron Variant LOC105372059 : Intron Variant | ND |
rs11697967 | chr20:32923896 | A>C / A>G | SNV | EFCAB8 : Intron Variant | AD |
rs11919880 | chr3:32920559 | A>G | SNV | Intergenic | AD |
rs4879635 | chr9:32899809 | G>A | SNV | APTX : Intron Variant | AD |
rs10122775 | chr9:32884985 | C>T | SNV | APTX : 3 Prime UTR Variant | AD |
rs4756329 | chr11:32883548 | T>A | SNV | Intergenic | AD |
rs10767971 | chr11:32874118 | T>C | SNV | Intergenic | AD |
rs6476383 | chr9:32865571 | A>G | SNV | Intergenic | ND |
rs2857103 | chr6:32823522 | C>A | SNV | TAP2 : Intron Variant | AD |
rs2621323 | chr6:32820930 | A>G | SNV | Intergenic | AD |
rs197710 | chr11:32816742 | A>G | SNV | Intergenic | AD |
rs990324 | chr13:32813108 | A>G | SNV | LINC00423 : Intron Variant | AD |
rs2424913 | chr20:32786453 | C>T | SNV | DNMT3B : Intron Variant | ND |
rs6743661 | chr2:32708028 | T>G | SNV | TTC27 : Intron Variant | AD |
rs2466046 | chr8:32659643 | G>A | SNV | NRG1 : Intron Variant | AD |
rs10941010 | chr5:32561694 | C>T | SNV | SUB1 : Intron Variant | AD |
rs17412116 | chr14:32497142 | G>A | SNV | AKAP6 : Intron Variant | AD |
rs4862932 | chr4:32475651 | T>C | SNV | LOC107986223 : Intron Variant | AD |
rs641221 | chr5:32439218 | A>G | SNV | ZFR : Intron Variant | AD |
rs4078204 | chr5:32275361 | G>A | SNV | MTMR12 : Intron Variant | AD |
rs8180531 | chr5:32215409 | T>C | SNV | Intergenic | AD |
rs11765220 | chr7:32203748 | C>T | SNV | PDE1C : Intron Variant | ND |
rs9825310 | chr3:32198627 | G>A | SNV | Intergenic | AD |
rs999 | chr6:32186109 | C>G | SNV | PBX2 : 3 Prime UTR Variant AGER : 2KB Upstream Variant | ND |
rs1800624 | chr6:32184610 | A>T | SNV | AGER : Non Coding Transcript Variant PBX2 : 500B Downstream Variant | AD |
rs4749705 | chr10:32131163 | C>T | SNV | Intergenic | AD |
rs73477 | chr10:32111468 | G>A / G>C | SNV | Intergenic | AD |
rs211424 | chr10:32109967 | T>C | SNV | Intergenic | AD |
rs211409 | chr10:32104285 | T>C | SNV | Intergenic | AD |
rs2405543 | chrX:32097024 | G>A | SNV | DMD : Intron Variant | AD |
rs2071293 | chr6:32094910 | G>A | SNV | TNXB : Intron Variant | AD |
rs7179733 | chr15:32081490 | C>T | SNV | CHRNA7 : Intron Variant | AD |
rs4747764 | chr10:32068628 | G>A | SNV | Intergenic | AD |
rs7766862 | chr6:32065230 | G>A | SNV | TNXB : Intron Variant | AD |
rs456053 | chr13:32061626 | G>A | SNV | FRY : Intron Variant | AD |
rs2214783 | chr7:32043563 | C>A | SNV | PDE1C : Intron Variant | ND |
rs1567887 | chr15:32007750 | C>T | SNV | Intergenic | AD |
rs17703610 | chr19:31980617 | A>C | SNV | LOC105372364 : Intron Variant LOC105372363 : Intron Variant | AD |
rs389883 | chr6:31979683 | G>T | SNV | STK19 : Intron Variant | AD |
rs386480 | chr6:31979060 | C>G | SNV | STK19 : Intron Variant | AD |
rs410851 | chr6:31968891 | T>C | SNV | SKIV2L : Synonymous Variant | AD |
rs7683244 | chr4:31965136 | G>T | SNV | Intergenic | AD |
rs437179 | chr6:31961237 | A>C | SNV | SKIV2L : Missense Variant | AD |
rs419788 | chr6:31961022 | T>C | SNV | SKIV2L : Intron VariantNELFE : 2KB Upstream Variant | AD |
rs630379 | chr6:31954477 | A>C | SNV | NELFE : Intron Variant | AD |
rs537160 | chr6:31948623 | A>G | SNV | CFB : Intron Variant | AD |
rs646370 | chr1:31935565 | A>G | SNV | PTP4A2 : Intron Variant | AD |
rs11770536 | chr7:31934361 | T>C | SNV | PDE1C : Intron Variant | ND |
rs10517232 | chr4:31934124 | T>C | SNV | Intergenic | AD |
rs591833 | chr1:31932289 | G>A | SNV | PTP4A2 : Intron Variant | AD |
rs13223209 | chr7:31910150 | G>A | SNV | PDE1C : Intron Variant | AD |
rs639233 | chr1:31907280 | C>T | SNV | PTP4A2 : Non Coding Transcript Variant | AD |
rs682654 | chr1:31905922 | C>A | SNV | PTP4A2 : 500B Downstream Variant | AD |
rs671101 | chr1:31870497 | A>G | SNV | Intergenic | AD |
rs1523145 | chr4:31862267 | T>C | SNV | Intergenic | AD |
rs4867084 | chr5:31818841 | G>A / G>C / G>T | SNV | PDZD2 : Intron Variant | AD |
rs929207 | chr16:31815894 | C>T | SNV | Intergenic | AD |
rs7731219 | chr5:31804466 | A>G | SNV | PDZD2 : Intron Variant | AD |
rs6811255 | chr4:31792028 | G>T | SNV | Intergenic | AD |
rs10029539 | chr4:31790330 | T>C | SNV | Intergenic | AD |
rs8082305 | chr17:31779568 | G>A | SNV | Intergenic | ND |
rs2219250 | chr3:31776052 | T>C | SNV | OSBPL10 : Intron Variant | AD |
rs7612780 | chr3:31769066 | A>G | SNV | OSBPL10 : Intron Variant | AD |
rs2168422 | chr3:31763350 | G>T | SNV | OSBPL10 : Intron Variant | AD |
rs9910565 | chr17:31758181 | A>T | SNV | Intergenic | AD |
rs253922 | chr5:31723153 | C>T | SNV | PDZD2 : Intron Variant | ND |
rs2833487 | chr21:31715550 | A>G | SNV | SCAF4 : Intron Variant | AD |
rs11944702 | chr4:31659117 | T>C | SNV | Intergenic | AD |
rs2173962 | chr21:31649707 | T>C | SNV | Intergenic | AD |
rs8128956 | chr21:31649104 | T>A / T>C | SNV | Intergenic | AD |
rs1667284 | chr18:31646245 | A>G | SNV | B4GALT6 : Intron Variant | AD |
rs11051507 | chr12:31642430 | C>A | SNV | Intergenic | ND |
rs6681414 | chr1:31604633 | G>A | SNV | Intergenic | AD |
rs6963296 | chr7:31576040 | T>C | SNV | CCDC129 : Intron Variant | ND |
rs2275435 | chr1:31425689 | C>T | SNV | SERINC2 : Intron Variant | AD |
rs4949402 | chr1:31425387 | T>C | SNV | SERINC2 : Synonymous Variant | AD |
rs1921968 | chrX:31419688 | C>T | SNV | DMD : Intron Variant | AD |
rs4478858 | chr1:31411078 | T>C | SNV | SERINC2 : Intron Variant | AD |
rs1039630 | chr1:31408625 | T>C | SNV | SERINC2 : 2KB Upstream Variant | AD |
rs2454908 | chr16:31399864 | C>T | SNV | ITGAD : Intron Variant | AD |
rs16932309 | chr10:31291676 | C>A | SNV | Intergenic | AD |
rs6884544 | chr5:31250481 | A>G | SNV | CDH6 : Intron Variant | AD |
rs7716554 | chr5:31200829 | G>A | SNV | CDH6 : Intron Variant | AD |
rs7953222 | chr12:31158141 | C>T | SNV | OVOS2 : Intron Variant | AD |
rs6487980 | chr12:31157874 | T>C | SNV | OVOS2 : Intron Variant | AD |
rs4943157 | chr13:31152041 | T>C | SNV | HSPH1 : Intron Variant | AD |
rs6917517 | chr6:31114584 | C>T | SNV | PSORS1C1 : 2KB Upstream Variant | AD |
rs12668955 | chr7:31076553 | G>A | SNV | ADCYAP1R1 : Intron Variant | AD |
rs17855121 | chr16:30992848 | T>C | SNV | STX1B : Synonymous Variant | AD |
rs3132580 | chr6:30952347 | G>A | SNV | DPCR1 : Missense Variant HCG21 : Intron Variant | AD |
rs3094086 | chr6:30951614 | G>A | SNV | DPCR1 : Synonymous Variant HCG21 : Intron Variant | AD |
rs3131921 | chr6:30939558 | T>C | SNV | DPCR1 : 2KB Upstream Variant | AD |
rs17600802 | chr13:30938017 | T>C | SNV | TEX26 : Intron Variant | AD |
rs179661 | chr14:30859665 | G>A | SNV | Intergenic | AD |
rs11612603 | chr12:30856623 | C>T | SNV | Intergenic | AD |
rs10813367 | chr9:30837983 | G>T | SNV | Intergenic | CD |
rs10229281 | chr7:30837026 | G>A | SNV | FAM188B : Intron Variant INMT-FAM188B : Intron Variant | ND |
rs33153 | chr12:30830904 | A>C | SNV | Intergenic | AD |
rs2114904 | chr12:30815728 | A>G | SNV | Intergenic | AD |
rs3129985 | chr6:30794765 | C>T | SNV | Intergenic | AD |
rs11765514 | chr7:30781314 | G>T | SNV | FAM188B : Intron Variant INMT-FAM188B : Intron Variant | AD |
rs10969853 | chr9:30751222 | T>C | SNV | Intergenic | AD |
rs11546742 | chr6:30724991 | C>G | SNV | TUBB : Non Coding Transcript Variant | AD |
rs2269705 | chr6:30689070 | T>C | SNV | NRM : Intron Variant PPP1R18 : 2KB Upstream Variant | AD |
rs2609954 | chr2:30648942 | G>A | SNV | CAPN13 : Intron Variant | AD |
rs3849883 | chr9:30639207 | G>A | SNV | Intergenic | AD |
rs449438 | chr11:30629472 | A>C / A>T | SNV | LOC105376609 : Intron Variant | AD |
rs17790906 | chr16:30558338 | T>G | SNV | ZNF764 : 2KB Upstream Variant | AD |
rs4952147 | chr2:30553404 | G>A | SNV | LCLAT1 : Intron Variant | AD |
rs11727470 | chr4:30542392 | A>G | SNV | Intergenic | AD |
rs8085261 | chr18:30531220 | A>C | SNV | Intergenic | ND |
rs1454979 | chr14:30525364 | C>A / C>T | SNV | LOC105370431 : Genic Upstream Transcript Variant | AD |
rs829646 | chr2:30496460 | T>C | SNV | LCLAT1 : Intron Variant | AD |
rs829642 | chr2:30477104 | T>C | SNV | LCLAT1 : Intron Variant | AD |
rs2037955 | chr7:30472333 | C>A | SNV | NOD1 : Intron Variant | AD |
rs13290610 | chr9:30460549 | A>G | SNV | Intergenic | AD |
rs10118000 | chr9:30460165 | G>A | SNV | Intergenic | AD |
rs2077164 | chr3:30290858 | A>G | SNV | Intergenic | AD |
rs58267302 | chr1:30259150 | T>C | SNV | LOC105378618 : Intron Variant | AD |
rs59765152 | chr1:30218970 | C>T | SNV | Intergenic | AD |
rs13375139 | chr1:30218866 | C>T | SNV | Intergenic | AD |
rs930321 | chr11:30144349 | T>A / T>C | SNV | LOC105376607 : Intron Variant | AD |
rs9314995 | chr13:30070281 | G>T | SNV | Intergenic | ND |
rs16833203 | chr1:30061036 | C>T | SNV | Intergenic | ND |
rs9297181 | chr8:30019089 | G>A | SNV | Intergenic | AD |
rs309853 | chr8:30016087 | A>G | SNV | Intergenic | AD |
rs4520995 | chr2:29895520 | T>C | SNV | ALK : Intron Variant | AD |
rs1108402 | chr7:29877002 | C>G / C>T | SNV | WIPF3 : Intron Variant | ND |
rs3218065 | chr19:29821675 | G>A | SNV | CCNE1 : Intron Variant | AD |
rs2229515 | chr15:29726423 | T>C | SNV | TJP1 : Missense Variant | ND |
rs1611371 | chr6:29712244 | C>T | SNV | Intergenic | AD |
rs1610594 | chr6:29711270 | C>T | SNV | Intergenic | AD |
rs1736931 | chr6:29710100 | A>C / A>T | SNV | Intergenic | AD |
rs17683205 | chr15:29709124 | C>T | SNV | TJP1 : Intron Variant | ND |
rs1476572 | chr6:29706964 | G>T | SNV | Intergenic | AD |
rs3131863 | chr6:29705706 | G>A | SNV | Intergenic | AD |
rs2394660 | chr6:29704909 | A>G | SNV | Intergenic | AD |
rs10519663 | chr15:29687136 | A>C | SNV | LOC105370743 : Non Coding Transcript Variant | ND |
rs8102949 | chr19:29681434 | T>C | SNV | Intergenic | AD |
rs187954 | chr1:29661757 | C>A / C>G | SNV | LOC107984934 : Intron Variant | ND |
rs502545 | chr1:29636635 | G>A | SNV | LOC107984934 : Intron Variant | AD |
rs62392942 | chr6:29634161 | T>C | SNV | GABBR1 : 2KB Upstream Variant | ND |
rs56020557 | chr6:29596985 | C>T | SNV | Intergenic | ND |
rs7079620 | chr10:29583020 | G>A | SNV | SVIL : Intron Variant | AD |
rs12473275 | chr2:29562915 | G>A | SNV | ALK : Intron Variant | AD |
rs10193521 | chr2:29562813 | G>A | SNV | ALK : Intron Variant | AD |
rs7592571 | chr2:29545028 | C>A / C>T | SNV | ALK : Intron Variant | AD |
rs12467802 | chr2:29524308 | C>G / C>T | SNV | ALK : Intron Variant | AD |
rs7580476 | chr2:29460692 | C>T | SNV | ALK : Intron Variant | AD |
rs1438339 | chr3:29440555 | C>T | SNV | RBMS3 : Intron Variant | AD |
rs10423905 | chr19:29437946 | A>C / A>T | SNV | LOC284395 : Intron Variant | AD |
rs4130687 | chr3:29402620 | A>G | SNV | RBMS3 : Intron Variant | ND |
rs3812350 | chr7:29282967 | G>C | SNV | CHN2 : Intron Variant | ND |
rs1543660 | chr13:29281513 | T>C | SNV | MTUS2 : Intron Variant | AD |
rs39109 | chr7:29279650 | C>T | SNV | CHN2 : Intron Variant | ND |
rs12617579 | chr2:29266754 | C>T | SNV | ALK : Intron Variant | ND |
rs9877517 | chr3:29246160 | G>A | SNV | Intergenic | AD |
rs2832278 | chr21:29239169 | A>G | SNV | LINC00189 : Intron Variant | AD |
rs11909745 | chr21:29238300 | A>G | SNV | LINC00189 : Intron Variant | AD |
rs17685936 | chr19:29155013 | A>G | SNV | Intergenic | AD |
rs13238274 | chr7:29140719 | C>T | SNV | CPVL : Intron Variant | AD |
rs7212295 | chr17:29104407 | A>G | SNV | MYO18A : Intron Variant | AD |
rs8037972 | chr15:29094390 | G>A | SNV | APBA2 : Intron Variant | AD |
rs7776819 | chr7:29091146 | A>G | SNV | CPVL : Intron Variant | AD |
rs12587874 | chr14:28984835 | A>G | SNV | LOC105370425 : Intron Variant | ND |
rs327127 | chr13:28944763 | C>G | SNV | MTUS2 : Intron Variant | ND |
rs2190305 | chr7:28819833 | A>G | SNV | CREB5 : Non Coding Transcript Variant | AD |
rs2237361 | chr7:28792680 | T>C / T>G | SNV | CREB5 : Intron Variant | ND |
rs4719953 | chr7:28774165 | T>A | SNV | CREB5 : Intron Variant | AD |
rs7021597 | chr9:28708153 | A>C | SNV | LINGO2 : Intron Variant | ND |
rs11747943 | chr5:28696483 | A>G | SNV | Intergenic | AD |
rs16897978 | chr5:28696397 | C>A | SNV | Intergenic | AD |
rs4398388 | chr3:28695131 | G>A | SNV | LINC00693 : Intron Variant | AD |
rs16874653 | chr7:28675439 | A>G | SNV | CREB5 : Intron Variant | AD |
rs6719289 | chr2:28633935 | A>G | SNV | PLB1 : Intron Variant | ND |
rs11127182 | chr2:28628249 | A>G | SNV | PLB1 : Intron Variant | ND |
rs10968666 | chr9:28603942 | A>G | SNV | LINGO2 : Intron Variant LOC105376004 : Non Coding Transcript Variant | AD |
rs12348435 | chr9:28600144 | A>C | SNV | LINGO2 : Intron Variant LOC105376004 : Non Coding Transcript Variant | AD |
rs9508066 | chr13:28578368 | G>A | SNV | LOC105370135 : Intron Variant | AD |
rs9550377 | chr13:28527544 | C>T | SNV | Intergenic | AD |
rs7085106 | chr10:28445426 | C>T | SNV | LOC105376468 : Intron Variant | ND |
rs7865532 | chr9:28407494 | T>C | SNV | LINGO2 : Intron Variant | AD |
rs10506030 | chr12:28362948 | A>T | SNV | CCDC91 : Intron Variant | AD |
rs7981680 | chr13:28319733 | C>G | SNV | FLT1 : Intron Variant | AD |
rs11706542 | chr3:28287092 | C>T | SNV | CMC1 : Intron Variant | AD |
rs6005754 | chr22:28286628 | T>C | SNV | TTC28 : Intron Variant | ND |
rs6487673 | chr12:28285474 | T>C | SNV | CCDC91 : Intron Variant | AD |
rs11564346 | chr18:28246998 | C>T | SNV | Intergenic | AD |
rs9310862 | chr3:28165386 | G>A | SNV | Intergenic | AD |
rs6803625 | chr3:28147258 | C>G | SNV | Intergenic | AD |
rs4749301 | chr10:28084715 | T>C | SNV | MPP7 : Intron Variant | AD |
rs4640131 | chr15:28014717 | A>G | SNV | OCA2 : Intron Variant | AD |
rs7317159 | chr13:28012083 | T>C | SNV | FLT3 : Intron Variant | AD |
rs17086213 | chr13:28010607 | T>C | SNV | FLT3 : Intron Variant | AD |
rs17567131 | chr15:28006367 | G>A | SNV | OCA2 : Intron Variant | AD |
rs7137085 | chr12:27932196 | G>A | SNV | Intergenic | AD |
rs2215263 | chr19:27923668 | T>A / T>C | SNV | Intergenic | AD |
rs10414401 | chr19:27921063 | C>T | SNV | Intergenic | AD |
rs811033 | chr19:27915321 | G>A | SNV | Intergenic | AD |
rs811029 | chr19:27912644 | A>G | SNV | Intergenic | AD |
rs7258218 | chr19:27908212 | C>A | SNV | LOC105372347 : 2KB Upstream Variant | AD |
rs4804973 | chr19:27902048 | G>A | SNV | LOC105372347 : Intron Variant | AD |
rs7255207 | chr19:27895015 | C>T | SNV | LOC105372347 : Intron Variant | AD |
rs16968523 | chr19:27893795 | C>T | SNV | LOC105372347 : Intron Variant | AD |
rs2333191 | chr14:27889693 | A>G | SNV | Intergenic | AD |
rs258430 | chr12:27880569 | A>G | SNV | Intergenic | AD |
rs9944711 | chr18:27847010 | T>C | SNV | Intergenic | CD |
rs915175 | chr10:27844758 | C>T | SNV | ARMC4 : Intron Variant | ND |
rs4525572 | chr18:27836281 | A>G | SNV | Intergenic | CD |
rs10137287 | chr14:27824902 | G>A | SNV | Intergenic | AD |
rs7311374 | chr12:27806972 | C>T | SNV | Intergenic | AD |
rs927848 | chr13:27803002 | A>G | SNV | Intergenic | AD |
rs16944011 | chr18:27712399 | C>G | SNV | Intergenic | ND |
rs12677898 | chr8:27655269 | A>G | SNV | SCARA3 : Intron Variant | AD |
rs4983262 | chr14:27651788 | T>C | SNV | LOC728755 : Intron Variant | AD |
rs10130248 | chr14:27650395 | A>G | SNV | LOC728755 : Intron Variant | AD |
rs17665021 | chr18:27642247 | T>G | SNV | Intergenic | ND |
rs16985179 | chr22:27633571 | C>T | SNV | Intergenic | AD |
rs2279591 | chr8:27596246 | C>T | SNV | EPHX2 : Intron Variant | ND |
rs4598563 | chr10:27576644 | A>G | SNV | LOC105376463 : Intron Variant | AD |
rs17778162 | chr17:27523483 | G>A | SNV | KSR1 : Intron Variant | AD |
rs1058326 | chr9:27447091 | G>A | SNV | MOB3B : Intron Variant | AD |
rs2589053 | chr9:27441539 | C>T | SNV | MOB3B : Intron Variant | AD |
rs28668284 | chr15:27364047 | G>A | SNV | GABRG3 : Intron Variant | AD |
rs10083616 | chr15:27364025 | G>A | SNV | GABRG3 : Intron Variant | AD |
rs9707971 | chr15:27363004 | A>G | SNV | GABRG3 : Intron Variant | AD |
rs9512637 | chr13:27346474 | T>C | SNV | Intergenic | AD |
rs1456796 | chr14:27341265 | A>C | SNV | LOC728755 : Intron Variant | ND |
rs2094497 | chr13:27335985 | T>C | SNV | Intergenic | AD |
rs2045935 | chr11:27316296 | A>G | SNV | Intergenic | OD |
rs1478684 | chr11:27315798 | T>G | SNV | Intergenic | OD |
rs11080131 | chr17:27309928 | T>G | SNV | WSB1 : Intron Variant | AD |
rs7479309 | chr11:27290267 | A>G | SNV | Intergenic | OD |
rs7468695 | chr9:27234523 | G>A | SNV | Intergenic | AD |
rs1590255 | chr9:27233970 | G>T | SNV | Intergenic | AD |
rs235938 | chr21:27224574 | T>C | SNV | LOC102724355 : Intron Variant LOC105372759 : Intron Variant | AD |
rs7091723 | chr10:27177236 | C>A | SNV | MASTL : Intron Variant | AD |
rs7336237 | chr13:27174157 | A>G | SNV | USP12-AS2 : Intron Variant | AD |
rs1522153 | chr3:27129286 | G>A | SNV | NEK10 : Intron Variant | AD |
rs6766181 | chr3:27058799 | C>T | SNV | Intergenic | AD |
rs9512491 | chr13:27012736 | G>A / G>C | SNV | Intergenic | AD |
rs4732900 | chr8:26820138 | T>A / T>C | SNV | ADRA1A : Intron Variant | CD |
rs10767583 | chr11:26805163 | C>T | SNV | Intergenic | AD |
rs4822791 | chr22:26790358 | G>A | SNV | Intergenic | AD |
rs2479505 | chr13:26756816 | T>A / T>C / T>G | SNV | GPR12 : 3 Prime UTR Variant | AD |
rs1752653 | chr13:26748640 | T>C | SNV | Intergenic | AD |
rs10519567 | chr15:26738703 | G>A / G>T | SNV | GABRB3 : Intron Variant | ND |
rs647852 | chr18:26734543 | A>G / A>T | SNV | Intergenic | AD |
rs10812450 | chr9:26722840 | C>T | SNV | LOC105376000 : Non Coding Transcript Variant | AD |
rs1955838 | chr14:26694881 | T>C | SNV | NOVA1-AS1 : Intron Variant | AD |
rs1950419 | chr14:26684854 | T>C | SNV | NOVA1-AS1 : Intron Variant | AD |
rs1009273 | chr10:26666669 | A>G | SNV | LOC105376462 : Intron Variant | AD |
rs372255102 | chr21:26630728 | T>C | SNV | Intergenic | AD |
rs2071862 | chr22:26625437 | G>A | SNV | CRYBA4 : Intron Variant | AD |
rs4822743 | chr22:26585075 | A>G | SNV | TPST2 : Intron Variant | AD |
rs763090 | chr22:26574051 | T>C | SNV | TPST2 : Intron Variant | ND |
rs2283839 | chr22:26573096 | A>C | SNV | TPST2 : Intron Variant | AD |
rs2283825 | chr22:26528569 | C>T | SNV | TPST2 : Intron Variant | AD |
rs2283822 | chr22:26528346 | C>T | SNV | TPST2 : Intron Variant | AD |
rs134157 | chr22:26520756 | C>T | SNV | Intergenic | AD |
rs5761557 | chr22:26482058 | A>G | SNV | HPS4 : Non Coding Transcript Variant SRRD : 2KB Upstream Variant | AD |
rs2280515 | chr2:26454435 | G>T | SNV | DRC1 : Intron Variant | AD |
rs11614384 | chr12:26383828 | T>C | SNV | ITPR2 : Intron Variant | AD |
rs667577 | chr22:26378614 | A>G | SNV | SEZ6L : Intron Variant | AD |
rs3808565 | chr8:26370124 | A>G | SNV | PPP2R2A : Intron Variant | AD |
rs11029525 | chr11:26334327 | A>C | SNV | ANO3 : Intron Variant | AD |
rs6519647 | chr22:26317998 | G>A / G>T | SNV | SEZ6L : Intron Variant | AD |
rs10070748 | chr5:26315360 | A>C | SNV | Intergenic | CD |
rs1800562 | chr6:26092913 | G>A | SNV | HFE : Missense Variant | AD |
rs2830045 | chr21:26086093 | A>G | SNV | APP : Intron Variant | AD |
rs6810498 | chr4:26064749 | A>G | SNV | Intergenic | AD |
rs4269167 | chr4:26024134 | T>C | SNV | Intergenic | AD |
rs7276036 | chr21:25989391 | G>A | SNV | APP : Intron Variant | AD |
rs11984569 | chr8:25977452 | G>T | SNV | EBF2 : Intron Variant | AD |
rs1324408 | chr13:25942322 | A>G | SNV | ATP8A2 : Intron Variant | AD |
rs184249 | chr13:25935931 | G>A | SNV | ATP8A2 : Intron Variant | AD |
rs12418699 | chr11:25825342 | T>C | SNV | LOC105376596 : Intron Variant | AD |
rs6484176 | chr11:25766084 | T>C | SNV | LOC105376596 : Intron Variant | ND |
rs4770875 | chr13:25745589 | A>G | SNV | ATP8A2 : Intron Variant | ND |
rs10431903 | chr16:25744980 | G>A | SNV | HS3ST4 : Intron Variant | ND |
rs9634421 | chr13:25735110 | G>A | SNV | ATP8A2 : Intron Variant | AD |
rs400196 | chr5:25717398 | A>G | SNV | Intergenic | AD |
rs10764581 | chr10:25707172 | T>A / T>C | SNV | LINC00836 : Intron Variant | AD |
rs17685787 | chr13:25688042 | A>G | SNV | ATP8A2 : Intron Variant | AD |
rs4144931 | chr9:25658152 | C>T | SNV | Intergenic | AD |
rs1286665 | chr3:25534184 | C>T | SNV | RARB : Intron Variant | AD |
rs10771224 | chr12:25506738 | T>C | SNV | LMNTD1 : Intron Variant | AD |
rs3005191 | chr10:25487247 | A>G | SNV | GPR158 : Intron Variant | AD |
rs1120839 | chr21:25442104 | G>A | SNV | Intergenic | ND |
rs2829746 | chr21:25425777 | G>A | SNV | LINC00158 : Intron Variant | ND |
rs13378890 | chr13:25422552 | C>T | SNV | ATP8A2 : Intron Variant | AD |
rs2345546 | chr16:25416151 | C>T | SNV | Intergenic | AD |
rs2829735 | chr21:25413995 | C>A | SNV | LINC00158 : Intron Variant | ND |
rs2829729 | chr21:25397616 | T>C | SNV | LINC00158 : Intron Variant | ND |
rs59551326 | chr21:25384656 | A>G | SNV | Intergenic | AD |
rs16894266 | chr5:25258761 | A>G | SNV | LOC105374693 : Intron Variant | ND |
rs7226622 | chr18:25211594 | C>T | SNV | ZNF521 : Intron Variant | AD |
rs9581297 | chr13:25209944 | G>T | SNV | Intergenic | AD |
rs1909475 | chr4:25198962 | T>C | SNV | SEPSECS-AS1 : 500B Downstream Variant LOC105374535 : Intron Variant | AD |
rs13106651 | chr4:25181823 | A>G | SNV | SEPSECS-AS1 : Intron Variant | AD |
rs1340000 | chr10:25171834 | G>A / G>T | SNV | GPR158-AS1 : Intron Variant | AD |
rs7530932 | chr1:25140670 | G>A | SNV | Intergenic | AD |
rs1979522 | chr12:25090959 | C>T | SNV | LRMP : Intron Variant | ND |
rs2829538 | chr21:25090761 | T>C | SNV | Intergenic | AD |
rs8114108 | chr20:25051439 | T>C | SNV | ACSS1 : Intron Variant | AD |
rs11047768 | chr12:25027124 | G>A | SNV | LOC645177 : Intron Variant | AD |
rs2950347 | chr8:25005194 | T>G | SNV | LOC105379330 : Intron Variant | ND |
rs17000583 | chr21:24967885 | A>G | SNV | LOC339622 : Intron Variant | AD |
rs5760740 | chr22:24926206 | C>G | SNV | SGSM1 : 3 Prime UTR Variant | ND |
rs139724 | chr22:24888862 | A>G | SNV | SGSM1 : Intron Variant | ND |
rs7078551 | chr10:24885797 | C>T | SNV | PRTFDC1 : Intron Variant | AD |
rs1389221 | chr5:24884151 | T>C | SNV | Intergenic | AD |
rs3131513 | chr1:24866664 | G>A | SNV | Intergenic | AD | ND |
rs4256430 | chr6:24862847 | G>A | SNV | FAM65B : Intron Variant | AD |
rs6516643 | chr21:24850084 | T>C | SNV | LOC339622 : Intron Variant | AD |
rs11700693 | chr21:24842731 | C>G / C>T | SNV | LOC339622 : Intron Variant | AD |
rs5996775 | chr22:24842325 | C>T | SNV | SGSM1 : Intron Variant | ND |
rs10834489 | chr11:24816255 | C>T | SNV | LUZP2 : Intron Variant | ND |
rs9323560 | chr14:24803720 | G>A | SNV | Intergenic | AD |
rs13336754 | chr16:24790658 | C>A / C>T | SNV | TNRC6A : Missense Variant | AD |
rs10834476 | chr11:24752960 | T>C | SNV | LUZP2 : Intron Variant | AD |
rs6482428 | chr10:24740234 | T>C | SNV | Intergenic | AD |
rs4246224 | chr12:24631205 | G>A | SNV | LOC105369698 : Intron Variant | AD |
rs6049811 | chr20:24609154 | T>C / T>G | SNV | SYNDIG1 : Intron Variant | AD |
rs9819865 | chr3:24595033 | G>A / G>C | SNV | Intergenic | AD |
rs6795607 | chr3:24589674 | T>C | SNV | Intergenic | AD |
rs17203601 | chr18:24577590 | G>A | SNV | Intergenic | AD |
rs11028019 | chr11:24562345 | T>C | SNV | LUZP2 : Intron Variant | ND |
rs499468 | chr18:24519685 | C>T | SNV | Intergenic | AD |
rs4748949 | chr10:24514128 | G>A | SNV | KIAA1217 : Intron Variant | AD |
rs537069 | chr18:24509280 | G>A | SNV | Intergenic | AD |
rs7927293 | chr11:24506412 | A>G | SNV | LUZP2 : Intron Variant | AD |
rs3797173 | chr5:24497138 | A>C / A>G / A>T | SNV | CDH10 : Intron Variant | ND |
rs6138298 | chr20:24447649 | C>A / C>T | SNV | Intergenic | AD |
rs677213 | chr18:24447024 | C>T | SNV | IMPACT : Intron Variant | ND |
rs2366915 | chr10:24418740 | C>T | SNV | KIAA1217 : Intron Variant | AD |
rs7309268 | chr12:24407310 | G>T | SNV | SOX5 : Intron Variant | AD |
rs9935277 | chr16:24373390 | A>G | SNV | Intergenic | AD |
rs550338 | chr12:24359103 | G>A | SNV | SOX5 : Intron Variant | AD |
rs1532010 | chr18:24348077 | G>A / G>T | SNV | OSBPL1A : Intron Variant | ND |
rs4609598 | chr11:24346342 | C>A / C>T | SNV | Intergenic | AD |
rs2295310 | chr14:24291049 | C>T | SNV | DHRS1 : Intron Variant LOC102725044 : Intron Variant | AD |
rs4568 | chr14:24290803 | G>A | SNV | DHRS1 : 3 Prime UTR Variant LOC102725044 : Intron Variant | AD |
rs4281802 | chr18:24226736 | T>C | SNV | OSBPL1A : Intron Variant | AD |
rs1357251 | chr12:24222667 | T>C | SNV | SOX5 : Intron Variant LOC101928471 : 2KB Upstream Variant | AD |
rs17203129 | chr18:24212686 | G>A | SNV | OSBPL1A : Intron Variant | AD |
rs16860738 | chr1:24205654 | T>C | SNV | LOC284632 : Intron Variant | AD |
rs12445719 | chr16:24202266 | T>C | SNV | PRKCB : Intron Variant MIR1273H : 2KB Upstream Variant | ND |
rs17398828 | chr21:24190721 | T>A / T>G | SNV | Intergenic | AD |
rs4648940 | chr1:24148687 | C>T | SNV | Intergenic | AD |
rs2238493 | chr16:24145625 | T>C | SNV | PRKCB : Intron Variant | AD |
rs5949232 | chrX:24145170 | G>A / G>T | SNV | Intergenic | AD |
rs7982678 | chr13:24144267 | G>A | SNV | SPATA13 : Intron Variant | AD |
rs11047279 | chr12:24140368 | C>T | SNV | SOX5 : Intron Variant | ND |
rs4276859 | chr1:24089643 | C>T | SNV | MYOM3 : Synonymous Variant | AD |
rs736081 | chr13:24085587 | T>C | SNV | SPATA13 : Intron Variant | AD |
rs9805786 | chr13:24084217 | G>T | SNV | SPATA13 : Intron Variant | AD |
rs2305024 | chr18:24082852 | A>C | SNV | TTC39C : Intron Variant | ND |
rs647381 | chr4:24058982 | A>G | SNV | PPARGC1A : Intron Variant | AD |
rs7540557 | chr1:24051454 | T>C | SNV | LOC107984931 : Intron Variant | AD |
rs11586125 | chr1:24050836 | T>C | SNV | LOC107984931 : Intron Variant | AD |
rs7761213 | chr6:24028175 | T>C | SNV | Intergenic | AD |
rs7553231 | chr1:24020613 | T>C | SNV | LOC105376863 : Intron Variant | AD |
rs12229376 | chr12:23976502 | G>T | SNV | SOX5 : Intron Variant | AD |
rs11047179 | chr12:23969997 | C>T | SNV | SOX5 : Intron Variant | AD |
rs518587 | chr6:23934217 | A>G | SNV | Intergenic | AD |
rs17784945 | chr8:23833760 | A>G | SNV | Intergenic | AD |
rs2267032 | chr22:23806086 | A>G | SNV | SMARCB1 : Intron Variant | AD |
rs12666547 | chr7:23792484 | C>A | SNV | STK31 : Intron Variant | AD |
rs2195731 | chr9:23785969 | C>A | SNV | ELAVL2 : Intron Variant | OD |
rs8126263 | chr20:23785640 | C>T | SNV | Intergenic | AD |
rs10483282 | chr14:23784487 | T>G | SNV | Intergenic | AD |
rs1561105 | chr8:23753286 | T>G | SNV | LOC107986930 : Intron Variant | AD |
rs4134385 | chr20:23744382 | A>G | SNV | Intergenic | AD |
rs13338358 | chr16:23742877 | G>A | SNV | Intergenic | AD |
rs4748908 | chr10:23725193 | A>G | SNV | KIAA1217 : Intron Variant | AD |
rs11577033 | chr1:23711741 | T>C | SNV | Intergenic | AD |
rs1491377 | chr4:23700935 | A>G | SNV | Intergenic | ND |
rs2828434 | chr21:23697122 | G>T | SNV | Intergenic | ND |
rs4769281 | chr13:23681651 | A>G / A>T | SNV | LOC105370114 : Non Coding Transcript Variant | AD |
rs11013645 | chr10:23680279 | A>G | SNV | Intergenic | AD |
rs11013643 | chr10:23679454 | A>G | SNV | Intergenic | AD |
rs10519442 | chr15:23663540 | A>G | SNV | Intergenic | AD |
rs6793612 | chr3:23642821 | C>T | SNV | Intergenic | AD |
rs6677615 | chr1:23616312 | G>A | SNV | Intergenic | AD |
rs16892567 | chr5:23579631 | G>A | SNV | Intergenic | AD |
rs10511730 | chr9:23563774 | C>G / C>T | SNV | LOC101929563 : Intron Variant | AD |
rs17089358 | chr8:23553762 | T>C | SNV | SLC25A37 : Intron Variant | AD |
rs6889665 | chr5:23532534 | T>C | SNV | Intergenic | AD |
rs10842176 | chr12:23521323 | G>A | SNV | Intergenic | AD |
rs7522616 | chr1:23468421 | A>G | SNV | ASAP3 : Intron Variant | AD |
rs17078717 | chr13:23410292 | A>G / A>T | SNV | SACS : Intron Variant | AD |
rs17078678 | chr13:23383375 | C>A | SNV | SACS : Intron Variant | AD |
rs2886497 | chr10:23381413 | G>C / G>T | SNV | Intergenic | AD |
rs9888818 | chr16:23288439 | G>A | SNV | SCNN1B : Intron Variant | AD |
rs4502928 | chr6:23214002 | A>G | SNV | Intergenic | AD |
rs9460842 | chr6:23200660 | C>G / C>T | SNV | Intergenic | AD |
rs4770403 | chr13:23180988 | G>A | SNV | SGCG : Intron Variant | AD |
rs1320561 | chr20:23117243 | G>A | SNV | Intergenic | AD |
rs11013291 | chr10:23111262 | T>C | SNV | MSRB2 : Intron Variant | AD |
rs3913141 | chr12:23040168 | G>A | SNV | Intergenic | AD |
rs1832047 | chr1:22940446 | G>A | SNV | Intergenic | AD |
rs3764213 | chr15:22845401 | G>C | SNV | NIPA2 : Intron Variant | ND |
rs439863 | chr4:22831059 | A>G | SNV | Intergenic | AD |
rs6659914 | chr1:22819906 | A>C | SNV | EPHB2 : Intron Variant | ND |
rs6048354 | chr20:22800188 | A>G / A>T | SNV | Intergenic | AD |
rs6511383 | chr19:22774098 | C>T | SNV | ZNF99 : Intron Variant | AD |
rs12974988 | chr19:22743163 | G>T | SNV | Intergenic | AD |
rs17350791 | chr12:22731542 | T>C | SNV | LOC107984516 : Intron Variant | AD |
rs2179556 | chr6:22689022 | T>C | SNV | LOC105374972 : Intron Variant | AD |
rs34929064 | chr7:22688653 | T>C | SNV | Intergenic | AD |
rs2057019 | chr6:22686612 | C>T | SNV | LOC105374972 : Intron Variant | AD |
rs7250285 | chr19:22654306 | C>T | SNV | ZNF492 : Intron Variant | AD |
rs158761 | chr1:22627879 | C>A | SNV | Intergenic | AD |
rs1545837 | chr8:22620294 | T>C | SNV | CCAR2 : Non Coding Transcript Variant BIN3 : 500B Downstream Variant | AD |
rs2827634 | chr21:22603487 | G>A | SNV | Intergenic | AD |
rs7246048 | chr19:22592832 | T>C | SNV | Intergenic | AD |
rs16999432 | chr19:22589845 | C>T | SNV | Intergenic | AD |
rs2905347 | chr7:22580700 | A>G | SNV | Intergenic | AD |
rs534632 | chr9:22458981 | G>A | SNV | Intergenic | AD |
rs292476 | chr13:22458981 | A>G | SNV | Intergenic | AD |
rs3114717 | chr7:22452771 | C>T | SNV | STEAP1B : Intron Variant | AD |
rs16894341 | chr5:22344141 | T>C | SNV | CDH12 : Intron Variant | ND |
rs5951550 | chrX:22342067 | C>A | SNV | PTCHD1-AS : Intron Variant | AD |
rs2827312 | chr21:22259356 | G>T | SNV | LOC107985508 : Intron Variant | AD |
rs4783448 | chr16:22230112 | C>T | SNV | EEF2K : Intron Variant | AD |
rs2473250 | chr1:22211156 | A>G | SNV | Intergenic | AD |
rs17010983 | chr3:22188256 | C>A | SNV | ZNF385D : Intron Variant | AD |
rs17707505 | chr7:22118446 | C>T | SNV | RAPGEF5 : 3 Prime UTR Variant | AD |
rs11812890 | chr10:22052966 | T>C | SNV | Intergenic | AD |
rs726730 | chr6:21995879 | A>G | SNV | CASC15 : Intron Variant | AD |
rs9350404 | chr6:21994515 | A>G | SNV | CASC15 : Intron Variant | AD |
rs2827182 | chr21:21986113 | C>T | SNV | Intergenic | AD |
rs10743428 | chr12:21952634 | T>C | SNV | Intergenic | AD |
rs6996493 | chr8:21936097 | A>G | SNV | XPO7 : Intron Variant | AD |
rs1487814 | chr11:21928939 | T>C | SNV | LOC102723370 : Intron Variant LOC105376587 : Intron Variant | AD |
rs2336055 | chr3:21853595 | C>T | SNV | ZNF385D : Intron Variant | AD |
rs17839323 | chr5:21842327 | A>G | SNV | CDH12 : Synonymous Variant | ND |
rs9836784 | chr3:21841499 | G>A | SNV | ZNF385D : Intron Variant | AD |
rs8141815 | chr22:21837296 | G>A | SNV | MAPK1 : Intron Variant | AD |
rs4769172 | chr13:21828788 | T>G | SNV | Intergenic | AD |
rs2479808 | chr6:21824163 | C>T | SNV | CASC15 : Intron Variant | AD |
rs9580203 | chr13:21805341 | T>C / T>G | SNV | Intergenic | AD |
rs1606851 | chr3:21795935 | G>A | SNV | ZNF385D : Intron Variant | AD |
rs8131512 | chr21:21776930 | A>G | SNV | LINC01425 : Intron Variant | ND |
rs9639395 | chr7:21740047 | G>A / G>C | SNV | DNAH11 : Intron Variant | AD |
rs11712735 | chr3:21732777 | T>A | SNV | ZNF385D : Intron Variant | ND |
rs670821 | chr13:21730077 | C>T | SNV | Intergenic | AD |
rs4488861 | chr3:21695081 | G>A / G>T | SNV | ZNF385D : Intron Variant | AD |
rs12232841 | chr19:21674425 | T>G | SNV | Intergenic | AD |
rs263930 | chr13:21664523 | C>G | SNV | Intergenic | ND |
rs12700284 | chr7:21407271 | G>T | SNV | Intergenic | ND |
rs12736884 | chr1:21399012 | G>C | SNV | Intergenic | AD |
rs8126935 | chr21:21315260 | A>G | SNV | NCAM2 : Intron Variant | AD |
rs7279496 | chr21:21307316 | C>A | SNV | NCAM2 : Intron Variant | AD |
rs2218433 | chr21:21305454 | A>G | SNV | NCAM2 : Intron Variant | AD |
rs8127865 | chr21:21271400 | A>G | SNV | NCAM2 : Intron Variant | AD |
rs4605456 | chr21:21264514 | C>T | SNV | NCAM2 : Intron Variant | AD |
rs6082329 | chr20:21119497 | A>C | SNV | Intergenic | AD |
rs2826660 | chr21:21116096 | A>G / A>T | SNV | NCAM2 : Intron Variant | AD |
rs2826659 | chr21:21115536 | A>C / A>T | SNV | NCAM2 : Intron Variant | AD |
rs6047255 | chr20:21115295 | A>G | SNV | Intergenic | AD |
rs7980084 | chr12:21069946 | A>G | SNV | SLCO1B7 : Intron Variant | AD |
rs1019233 | chr7:21048964 | C>T | SNV | Intergenic | ND |
rs11789272 | chr9:21030852 | G>A | SNV | HACD4 : Intron Variant LOC105375989 : Non Coding Transcript Variant | AD |
rs1400369 | chr11:20994749 | A>C | SNV | NELL1 : Intron Variant | AD |
rs10500885 | chr11:20993514 | T>C | SNV | NELL1 : Intron Variant | AD |
rs178260 | chr22:20970019 | G>T | SNV | AIFM3 : Intron Variant | ND |
rs6475490 | chr9:20945208 | G>C | SNV | FOCAD : Intron Variant | AD |
rs10841707 | chr12:20917203 | T>A | SNV | SLCO1B3 : 500B Downstream Variant | AD |
rs11825833 | chr11:20831700 | T>C | SNV | NELL1 : Intron Variant | AD |
rs10089021 | chr8:20781983 | T>C | SNV | LOC105379315 : Intron Variant | AD |
rs12664021 | chr6:20760849 | C>T | SNV | CDKAL1 : Intron Variant | ND |
rs1554368 | chr11:20754212 | A>G | SNV | NELL1 : Intron Variant | ND |
rs1996623 | chr11:20737870 | A>G | SNV | NELL1 : Intron Variant | ND |
rs170676 | chr21:20724023 | G>C | SNV | Intergenic | AD |
rs463877 | chr21:20717939 | T>C | SNV | Intergenic | AD |
rs2128345 | chr21:20713530 | A>G | SNV | Intergenic | AD |
rs229369 | chr21:20706272 | G>A | SNV | Intergenic | AD |
rs17809565 | chr3:20696597 | A>G / A>T | SNV | Intergenic | AD |
rs1500422 | chr3:20678646 | G>A / G>C | SNV | Intergenic | AD |
rs1013363 | chr2:20663526 | C>T | SNV | Intergenic | CD |
rs7570901 | chr2:20661447 | A>G | SNV | Intergenic | CD |
rs9295475 | chr6:20652534 | A>G | SNV | CDKAL1 : Intron Variant | ND |
rs2206579 | chr6:20625403 | A>G | SNV | CDKAL1 : Intron Variant | AD |
rs9506528 | chr13:20614200 | G>A | SNV | IFT88 : Intron Variant | AD |
rs12791734 | chr11:20595465 | T>A | SNV | Intergenic | AD |
rs12380857 | chr9:20578042 | T>C | SNV | MLLT3 : Intron Variant | ND |
rs7868755 | chr9:20551929 | C>T | SNV | MLLT3 : Intron Variant | ND |
rs2188873 | chr7:20486643 | G>A | SNV | Intergenic | AD |
rs3093927 | chr14:20354936 | G>A | SNV | PARP2 : Synonymous Variant | AD |
rs59730814 | chr11:20334799-20334811 | delA / dupA / dupAA | Indel | Intergenic | AD |
rs10498267 | chr14:20334156 | T>C | SNV | CCNB1IP1 : 2KB Upstream Variant | AD |
rs11128951 | chr3:20334054 | A>G | SNV | Intergenic | AD |
rs9871864 | chr3:20311274 | T>C | SNV | Intergenic | AD |
rs1551534 | chr9:20255357 | A>G | SNV | SLC24A2 : Intron Variant | AD |
rs877098 | chr13:20224101 | A>G | SNV | GJB6 : Intron Variant | AD |
rs11025421 | chr11:20177732 | C>A | SNV | Intergenic | AD |
rs17678713 | chr3:20151277 | G>A | SNV | KAT2B : Intron Variant | AD |
rs73602388 | chr8:20141801 | C>T | SNV | Intergenic | CD |
rs2483767 | chr6:20128326 | A>G | SNV | MBOAT1 : Intron Variant | AD |
rs1886712 | chr16:20072371 | C>G | SNV | GPR139 : Intron Variant | AD |
rs7141391 | chr14:20029578 | A>C / A>T | SNV | Intergenic | AD |
rs662751 | chr6:20027407 | A>G | SNV | Intergenic | AD |
rs11753077 | chr6:20014974 | T>A / T>G | SNV | Intergenic | AD |
rs2238796 | chr22:20011550 | C>A / C>T | SNV | ARVCF : Intron Variant | ND |
rs6586879 | chr8:19905221 | C>T | SNV | LOC107986921 : Intron Variant | AD |
rs9350195 | chr6:19899174 | T>A / T>C | SNV | Intergenic | AD |
rs4866159 | chr5:19892825 | T>C | SNV | CDH18 : Intron Variant | ND |
rs4461636 | chr5:19885107 | T>G | SNV | CDH18 : Intron Variant | ND |
rs1391429 | chr5:19848216 | A>G | SNV | CDH18 : Intron Variant | ND |
rs4242066 | chr5:19840836 | C>A | SNV | CDH18 : Intron Variant | ND |
rs6451476 | chr5:19827213 | T>G | SNV | CDH18 : Intron Variant | ND |
rs11908323 | chr20:19826835 | A>G | SNV | RIN2 : Intron Variant | ND |
rs6081761 | chr20:19826064 | G>A | SNV | RIN2 : Intron Variant | ND |
rs12527834 | chr6:19821550 | A>G | SNV | Intergenic | AD |
rs6983139 | chr8:19742818 | A>G | SNV | CSGALNACT1 : Intron Variant | AD |
rs11779629 | chr8:19654461 | A>T | SNV | CSGALNACT1 : Intron Variant | AD |
rs10494868 | chr10:19518946 | C>A | SNV | MALRD1 : Intron Variant | AD |
rs3852465 | chr10:19507501 | T>C | SNV | MALRD1 : Intron Variant | AD |
rs6481955 | chr10:19506116 | A>G | SNV | MALRD1 : Intron Variant | AD |
rs1386449 | chr11:19466536 | A>G | SNV | NAV2 : Intron Variant | AD |
rs1387616 | chr21:19454882 | A>G | SNV | Intergenic | AD |
rs1858504 | chr6:19214658 | C>T | SNV | Intergenic | AD |
rs16981939 | chr2:19177142 | T>C | SNV | Intergenic | CD |
rs11973510 | chr7:19171630 | C>A | SNV | Intergenic | AD |
rs8062326 | chr16:19144694 | G>A | SNV | Intergenic | AD |
rs10454701 | chr16:19143368 | A>G | SNV | Intergenic | CD |
rs7030400 | chr9:19014647 | C>A | SNV | SAXO1 : Intron Variant | AD |
rs884895 | chr2:19003723 | G>A | SNV | LINC01376 : Intron Variant | AD |
rs4912013 | chr1:18958070 | T>C | SNV | IFFO2 : 2KB Upstream Variant | AD |
rs6999315 | chr8:18937535 | A>G | SNV | PSD3 : Intron Variant | AD |
rs6081377 | chr20:18796142 | T>C | SNV | LINC00652 : 2KB Upstream Variant LOC100270804 : 500B Downstream Variant | AD |
rs9847248 | chr3:18763163 | G>A | SNV | LOC105376976 : Intron Variant | AD |
rs9284846 | chr3:18749210 | G>T | SNV | LOC105376976 : Intron Variant | AD |
rs2743189 | chr1:18729888 | C>T | SNV | PAX7 : Intron Variant | AD |
rs2062691 | chr5:18725285 | C>G | SNV | Intergenic | CD |
rs1867877 | chr11:18705901 | T>C | SNV | IGSF22 : Missense Variant LOC105376579 : 2KB Upstream Variant | AD |
rs9826966 | chr3:18696304 | A>G | SNV | LOC105376976 : 2KB Upstream Variant | AD |
rs9845140 | chr3:18687386 | C>A | SNV | Intergenic | AD |
rs1550771 | chr2:18679109 | T>C | SNV | LOC105373456 : Non Coding Transcript Variant | AD |
rs9975541 | chr21:18678255 | G>A | SNV | MIR548XHG : Intron Variant | AD |
rs11914608 | chr3:18662807 | A>G | SNV | Intergenic | AD |
rs9855153 | chr3:18651731 | A>G | SNV | Intergenic | AD |
rs336605 | chr3:18614858 | G>T | SNV | Intergenic | AD |
rs10963662 | chr9:18601141 | A>C | SNV | ADAMTSL1 : Intron Variant | AD |
rs334960 | chr3:18569385 | C>T | SNV | Intergenic | AD |
rs10120545 | chr9:18386759 | C>T | SNV | ADAMTSL1 : Intron Variant | AD |
rs12240995 | chr10:18348303 | A>C | SNV | CACNB2 : Intron Variant | ND |
rs10810935 | chr9:18251857 | A>G / A>T | SNV | ADAMTSL1 : Intron Variant | AD |
rs1277769 | chr10:18210865 | C>A | SNV | CACNB2 : Intron Variant | ND |
rs1033190 | chr1:18202354 | G>T | SNV | IGSF21 : Intron Variant | AD |
rs17198023 | chr9:18194385 | A>C | SNV | ADAMTSL1 : Intron Variant | ND |
rs2824695 | chr21:18186741 | A>G | SNV | CHODL : Intron Variant | ND |
rs34236855 | chr9:18178316 | G>A | SNV | ADAMTSL1 : Intron Variant | AD |
rs12006002 | chr9:18166901 | C>T | SNV | ADAMTSL1 : Intron Variant | AD |
rs2320289 | chr4:18160481 | A>C | SNV | Intergenic | AD |
rs763976 | chr9:18134916 | A>C | SNV | ADAMTSL1 : Intron Variant | AD |
rs2824642 | chr21:18131787 | C>G / C>T | SNV | CHODL : Intron Variant | ND |
rs10963462 | chr9:18130038 | G>T | SNV | ADAMTSL1 : Intron Variant | AD |
rs4813301 | chr20:18089684 | G>A | SNV | Intergenic | AD |
rs12255303 | chr10:18084057 | A>G | SNV | Intergenic | AD |
rs9291662 | chr4:18077894 | G>A | SNV | Intergenic | AD |
rs1563749 | chr4:18070877 | C>T | SNV | Intergenic | AD |
rs4920422 | chr1:18066258 | C>A | SNV | LOC101927876 : Intron Variant | AD |
rs74067914 | chr12:18036994 | T>C | SNV | Intergenic | AD |
rs1339934 | chr1:17909965 | A>G | SNV | Intergenic | AD |
rs60349741 | chr11:17774564 | A>C / A>T | SNV | KCNC1 : Intron Variant | OD |
rs4611850 | chr3:17757157 | T>A / T>G | SNV | Intergenic | AD |
rs4349529 | chr3:17750626 | A>G | SNV | Intergenic | AD |
rs6044991 | chr20:17746038 | A>G | SNV | Intergenic | AD |
rs7627732 | chr3:17743326 | T>C | SNV | TBC1D5 : 2KB Upstream Variant LOC105376975 : Intron Variant | AD |
rs4908967 | chr3:17733452 | C>A | SNV | TBC1D5 : Intron Variant | AD |
rs4757574 | chr11:17704827 | A>G | SNV | Intergenic | AD |
rs11128838 | chr3:17655876 | G>A | SNV | TBC1D5 : Intron Variant | AD |
rs2588112 | chr8:17618805 | C>G | SNV | PDGFRL : Intron Variant | ND |
rs9823767 | chr3:17574245 | A>G | SNV | TBC1D5 : Intron Variant | AD |
rs2249449 | chr21:17560125 | A>G / A>T | SNV | CXADR : Intron Variant | ND |
rs2249443 | chr21:17560034 | G>A | SNV | CXADR : Intron Variant | ND |
rs2249100 | chr21:17557426 | C>A | SNV | CXADR : Intron Variant | ND |
rs6602203 | chr10:17554122 | C>T | SNV | Intergenic | AD |
rs2477735 | chr1:17542684 | T>C | SNV | ARHGEF10L : Intron Variant | AD |
rs17380121 | chr2:17501964 | G>T | SNV | Intergenic | AD |
rs10840729 | chr12:17500900 | G>A | SNV | Intergenic | AD |
rs10219728 | chr12:17486887 | A>G | SNV | Intergenic | AD |
rs2441997 | chr9:17474087 | G>A | SNV | CNTLN : Intron Variant | AD |
rs1868361 | chr7:17456045 | C>T | SNV | KCCAT333 : Intron Variant LOC105375172 : Intron Variant | AD |
rs1305295 | chr12:17419308 | G>A | SNV | Intergenic | AD |
rs16982400 | chr22:17418497 | T>C | SNV | CECR2 : Intron Variant | ND |
rs4148646 | chr11:17393643 | C>G | SNV | ABCC8 : Intron Variant | AD |
rs7647905 | chr3:17391891 | T>C | SNV | TBC1D5 : Intron Variant | AD |
rs1374197 | chr3:17353123 | A>G | SNV | TBC1D5 : Intron Variant | AD |
rs400333 | chr10:17309795 | A>G | SNV | Intergenic | AD |
rs1578405 | chr20:17248099 | A>G | SNV | PCSK2 : Intron Variant LOC105372546 : Intron Variant | AD |
rs3818916 | chr20:17227076 | G>A / G>T | SNV | PCSK2 : Intron Variant LOC105372546 : 500B Downstream Variant | AD |
rs11667918 | chr19:17121689 | C>T | SNV | MYO9B : Intron Variant | AD |
rs10090288 | chr8:17072126 | A>C | SNV | MICU3 : Intron Variant | AD |
rs7058279 | chrX:17062593 | T>C | SNV | REPS2 : Intron Variant | AD |
rs17624782 | chr8:17058471 | G>T | SNV | MICU3 : Intron Variant | AD |
rs263548 | chr9:17028237 | C>A | SNV | LOC105375983 : Intron Variant | ND |
rs9876768 | chr3:17008473 | T>C | SNV | PLCL2 : Intron Variant | AD |
rs2353203 | chr19:16989170 | G>A | SNV | CPAMD8 : Intron Variant | AD |
rs823583 | chr8:16979690 | A>G | SNV | Intergenic | AD |
rs1721078 | chr8:16973425 | A>G | SNV | Intergenic | AD |
rs12249562 | chr10:16973406 | G>A | SNV | CUBN : Intron Variant | AD |
rs1721013 | chr7:16969977 | C>T | SNV | Intergenic | AD |
rs1473730 | chr6:16918319 | T>C | SNV | Intergenic | AD |
rs29452 | chr5:16910496 | C>A | SNV | MYO10 : Intron Variant | AD |
rs3740169 | chr10:16831548 | G>A / G>T | SNV | CUBN : Intron Variant | AD |
rs10063505 | chr5:16822062 | C>A | SNV | MYO10 : Intron Variant | AD |
rs12188582 | chr5:16818254 | A>G | SNV | MYO10 : Intron Variant | AD |
rs6778524 | chr3:16814451 | T>C | SNV | PLCL2 : Intron Variant | AD |
rs216495 | chr11:16812963 | G>A | SNV | PLEKHA7 : Intron Variant | ND |
rs115664995 | chr10:16796593 | G>T | SNV | RSU1 : Intron Variant | CD |
rs1580852 | chr8:16717603 | C>T | SNV | Intergenic | AD |
rs9860475 | chr3:16707517 | C>T | SNV | Intergenic | AD |
rs10097146 | chr8:16701221 | G>A | SNV | Intergenic | AD |
rs1075080 | chr21:16672334 | A>G | SNV | Intergenic | AD |
rs35004 | chr5:16617794 | C>A / C>T | SNV | FAM134B : 2KB Upstream Variant LOC101929524 : Intron Variant | AD |
rs5746647 | chr22:16576248 | G>T | SNV | Intergenic | AD |
rs994429 | chr5:16552290 | T>A / T>G | SNV | FAM134B : Intron Variant | CD |
rs2115066 | chr5:16550367 | C>A | SNV | FAM134B : Intron Variant | CD |
rs154791 | chr5:16448928 | G>A | SNV | Intergenic | AD |
rs1503452 | chr11:16430585 | C>T | SNV | SOX6 : Intron Variant | AD |
rs11603071 | chr11:16386702 | T>C | SNV | SOX6 : Intron Variant | AD |
rs1370465 | chr11:16372522 | G>A | SNV | SOX6 : Intron Variant | AD |
rs12656374 | chr5:16346463 | C>T | SNV | Intergenic | CD |
rs16934439 | chr9:16321580 | T>G | SNV | Intergenic | AD |
rs2582662 | chr5:16272528 | G>A | SNV | Intergenic | AD |
rs13340561 | chr8:16201396 | T>G | SNV | Intergenic | AD |
rs6080131 | chr20:16125395 | A>G | SNV | Intergenic | AD |
rs4148358 | chr16:16093318 | C>T | SNV | ABCC1 : Intron Variant | AD |
rs2074086 | chr16:16087285 | T>C | SNV | ABCC1 : Intron Variant | AD |
rs35626 | chr16:16076758 | G>T | SNV | ABCC1 : Intron Variant | AD |
rs1887671 | chr9:16035674 | T>C | SNV | CCDC171 : Intron Variant | AD |
rs924136 | chr16:16032618 | G>A / G>C | SNV | ABCC1 : Intron Variant | AD |
rs6706117 | chr2:15991660 | A>G | SNV | Intergenic | AD |
rs7251890 | chr19:15961227 | A>C | SNV | Intergenic | AD |
rs4685266 | chr3:15867259 | A>G | SNV | Intergenic | AD |
rs3794987 | chr19:15640081 | A>G | SNV | CYP4F3 : 2KB Upstream Variant | AD |
rs7256985 | chr19:15621260 | G>T | SNV | CYP4F8 : Intron Variant | AD |
rs2176918 | chr19:15620112 | A>G | SNV | CYP4F8 : Intron Variant | AD |
rs7254518 | chr19:15616955 | G>A | SNV | CYP4F8 : Intron Variant | AD |
rs10456773 | chr6:15537094 | T>C | SNV | DTNBP1 : Intron Variant LOC105374947 : Intron Variant | AD |
rs12495710 | chr3:15517721 | C>T | SNV | COLQ : Intron Variant | AD |
rs760659 | chr6:15504358 | T>C | SNV | JARID2 : Intron Variant | AD |
rs13271637 | chr8:15500300 | G>A / G>C | SNV | Intergenic | AD |
rs7013543 | chr8:15499544 | C>A | SNV | Intergenic | AD |
rs1390054 | chr8:15499026 | C>T | SNV | Intergenic | AD |
rs1390053 | chr8:15498946 | C>T | SNV | Intergenic | AD |
rs1390052 | chr8:15498875 | A>C | SNV | Intergenic | AD |
rs6530877 | chr8:15498525 | C>A / C>G / C>T | SNV | Intergenic | AD |
rs6985300 | chr8:15498160 | A>C | SNV | Intergenic | AD |
rs11023571 | chr11:15434922 | G>A / G>T | SNV | Intergenic | AD |
rs2496320 | chr1:15417775 | T>C | SNV | EFHD2 : Intron Variant | AD |
rs2496321 | chr1:15417388 | A>C | SNV | EFHD2 : Intron Variant | AD |
rs7867510 | chr9:15353412 | G>A | SNV | Intergenic | AD |
rs707838 | chr6:15352012 | G>T | SNV | JARID2 : Intron Variant | AD |
rs680686 | chr9:15351452 | A>G | SNV | Intergenic | AD |
rs1215130 | chr9:15343711 | C>T | SNV | Intergenic | AD |
rs6488769 | chr12:15310362 | C>T | SNV | Intergenic | AD |
rs1318937 | chr3:15253857 | A>G | SNV | SH3BP5-AS1 : 2KB Upstream Variant SH3BP5 : 500B Downstream Variant | AD | ND |
rs12311304 | chr12:15236703 | T>C | SNV | Intergenic | AD |
rs767201 | chr12:15217944 | G>A | SNV | RERG : Intron Variant | AD |
rs57126985 | chr21:15217712 | G>C | SNV | Intergenic | AD |
rs7955309 | chr12:15215264 | T>C | SNV | RERG : Intron Variant | AD |
rs4792581 | chr17:15163379 | T>C | SNV | Intergenic | AD |
rs982313 | chrX:15128650 | C>T | SNV | Intergenic | AD |
rs11078278 | chr17:15090684 | T>C | SNV | Intergenic | AD |
rs7529561 | chr1:15001655 | A>C | SNV | KAZN : Intron Variant | AD |
rs5980083 | chrX:14961643 | T>C | SNV | Intergenic | AD |
rs16930625 | chr11:14896762 | A>G | SNV | CYP2R1 : 5 Prime UTR Variant | AD |
rs1562902 | chr11:14896670 | C>T | SNV | CYP2R1 : 5 Prime UTR Variant | AD |
rs9916612 | chr17:14860247 | C>T | SNV | LOC107984977 : Intron Variant | AD |
rs1687320 | chr3:14853127 | C>A / C>G | SNV | FGD5 : Intron Variant | ND |
rs13070730 | chr3:14831707 | T>C | SNV | FGD5 : Intron Variant | AD |
rs1389733 | chr9:14791717 | G>T | SNV | FREM1 : Intron Variant LOC105375979 : 2KB Upstream Variant | AD |
rs2291681 | chr9:14790843 | G>T | SNV | FREM1 : Intron Variant | ND |
rs10117516 | chr9:14749436 | C>G / C>T | SNV | FREM1 : Intron Variant | AD |
rs12496846 | chr3:14731760 | A>G | SNV | C3orf20 : Intron Variant | OD |
rs25992 | chr5:14707491 | C>A / C>G / C>T | SNV | OTULIN : Intron Variant ANKH : 3 Prime UTR Variant | AD |
rs25952 | chr5:14695138 | A>C | SNV | OTULIN : Intron Variant | AD |
rs17155611 | chr10:14625354 | C>T | SNV | FAM107B : Intron Variant | CD |
rs17602660 | chr7:14606660 | A>T | SNV | DGKB : Intron Variant | AD |
rs11259210 | chr10:14591724 | T>C | SNV | FAM107B : Intron Variant | AD |
rs1409390 | chr10:14585847 | T>C | SNV | FAM107B : Intron Variant | AD |
rs760347 | chr21:14568068 | C>T | SNV | SAMSN1 : Intron Variant | AD |
rs6110333 | chr20:14568030 | C>T | SNV | MACROD2 : Intron Variant MACROD2-IT1 : Intron Variant | AD |
rs12425606 | chr12:14562859 | C>T | SNV | PLBD1 : Intron Variant | ND |
rs6079482 | chr20:14536574 | T>C | SNV | MACROD2 : Intron Variant | AD |
rs12446921 | chr16:14535631 | A>G | SNV | PARN : Intron Variant | AD |
rs732459 | chr16:14533837 | C>T | SNV | PARN : Intron Variant LOC107984865 : 2KB Upstream Variant | AD |
rs872526 | chr3:14519332 | A>C | SNV | GRIP2 : Intron Variant | ND |
rs13285597 | chr9:14483656 | C>T | SNV | Intergenic | AD |
rs35094112 | chr9:14483583 | G>A | SNV | Intergenic | AD |
rs35950138 | chr9:14483145 | C>T | SNV | Intergenic | AD |
rs3773165 | chr3:14482762 | G>A | SNV | SLC6A6 : Intron Variant | AD |
rs13299701 | chr9:14482458 | C>T | SNV | Intergenic | AD |
rs56327111 | chr9:14481384 | A>G | SNV | Intergenic | AD |
rs9834678 | chr3:14475607 | T>C | SNV | SLC6A6 : Intron Variant | AD |
rs2289128 | chr3:14472187 | G>A / G>C | SNV | SLC6A6 : Intron Variant | AD |
rs3773171 | chr3:14470585 | C>T | SNV | SLC6A6 : Intron Variant | AD |
rs3773172 | chr3:14470191 | G>A | SNV | SLC6A6 : Intron Variant | AD |
rs12489456 | chr3:14459666 | G>A | SNV | SLC6A6 : Intron Variant | AD |
rs17237132 | chr3:14457512 | C>T | SNV | SLC6A6 : Intron Variant | ND |
rs59677118 | chr9:14441679 | G>A | SNV | Intergenic | AD |
rs56037905 | chr9:14432028 | G>A | SNV | Intergenic | AD |
rs12638941 | chr3:14419407 | C>T | SNV | SLC6A6 : Intron Variant | ND |
rs2349300 | chr11:14352116 | T>C | SNV | RRAS2 : Intron Variant | AD |
rs2822589 | chr21:14339219 | T>C | SNV | Intergenic | AD |
rs2822586 | chr21:14337696 | T>C | SNV | Intergenic | AD |
rs2822582 | chr21:14337293 | T>G | SNV | Intergenic | AD |
rs2822573 | chr21:14332596 | A>G | SNV | Intergenic | AD |
rs11023186 | chr11:14321215 | G>A | SNV | RRAS2 : Intron Variant | AD |
rs2822567 | chr21:14319749 | C>T | SNV | Intergenic | AD |
rs8131875 | chr21:14315172 | A>G | SNV | Intergenic | AD |
rs887772 | chr21:14313131 | T>G | SNV | Intergenic | AD |
rs2382468 | chr9:14303062 | T>G | SNV | NFIB : Intron Variant | AD |
rs2822557 | chr21:14298703 | G>A | SNV | ABCC13 : Intron Variant | AD |
rs11023182 | chr11:14297284 | G>T | SNV | RRAS2 : Intron Variant | AD |
rs10928056 | chr1:14259153 | G>A | SNV | KAZN : Intron Variant | AD |
rs2303975 | chr11:14255453 | G>A | SNV | SPON1 : Intron Variant | AD |
rs731274 | chr11:14252131 | G>A | SNV | SPON1 : Intron Variant | AD |
rs6442433 | chr3:14234259 | C>G | SNV | Intergenic | AD |
rs2895596 | chr10:14224086 | A>G | SNV | FRMD4A : Intron Variant | AD |
rs8516 | chr3:14143169 | T>C | SNV | TMEM43 : 3 Prime UTR Variant | AD |
rs366563 | chr5:14106504 | G>T | SNV | Intergenic | AD |
rs446989 | chr5:14106062 | G>A | SNV | Intergenic | AD |
rs386450 | chr5:14106027 | A>G | SNV | Intergenic | AD |
rs656208 | chr5:14105739 | C>G / C>T | SNV | Intergenic | AD |
rs10116586 | chr9:14058549 | A>C | SNV | Intergenic | AD |
rs7249702 | chr19:14027400 | G>A | SNV | RLN3 : 2KB Upstream Variant | AD |
rs7247578 | chr19:14027335 | C>T | SNV | RLN3 : 2KB Upstream Variant | AD |
rs7251796 | chr19:14024844 | C>T | SNV | Intergenic | AD |
rs7727798 | chr5:13993421 | T>C | SNV | DNAH5 : Intron Variant | AD |
rs10055489 | chr5:13987357 | A>G | SNV | DNAH5 : Intron Variant | ND |
rs1031006 | chr5:13986994 | A>G | SNV | DNAH5 : Intron Variant | ND |
rs17292523 | chr5:13985770 | A>G | SNV | DNAH5 : Intron Variant | ND |
rs12575169 | chr11:13976261 | A>C | SNV | SPON1 : Intron Variant | AD |
rs2457861 | chr10:13964391 | G>A | SNV | FRMD4A : Intron Variant | ND |
rs2073290 | chr20:13849491 | A>C / A>T | SNV | SEL1L2 : Missense Variant | AD |
rs16902820 | chr5:13834597 | T>C / T>G | SNV | DNAH5 : Intron Variant | AD |
rs6134980 | chr20:13833963 | C>T | SNV | Intergenic | AD |
rs12610873 | chr19:13831773 | G>A | SNV | ZSWIM4 : 3 Prime UTR Variant | AD |
rs9955902 | chr18:13828445 | T>G | SNV | Intergenic | AD |
rs10939516 | chr4:13813531 | A>G | SNV | LINC01182 : Intron Variant LOC101929048 : Intron Variant | AD |
rs2014788 | chr1:13799958 | C>T | SNV | PRDM2 : Intron Variant | AD |
rs4763358 | chr12:13720757 | G>C | SNV | GRIN2B : Intron Variant | ND |
rs10939500 | chr4:13713497 | C>A | SNV | LINC01182 : Intron Variant LOC107986184 : Intron Variant | AD |
rs7313149 | chr12:13675353 | T>C | SNV | GRIN2B : Intron Variant | ND |
rs4797793 | chr18:13638963 | G>A | SNV | LDLRAD4 : Intron Variant | AD |
rs12423978 | chr12:13556918 | C>T | SNV | GRIN2B : 3 Prime UTR Variant | AD |
rs1864097 | chr5:13450684 | C>T | SNV | LOC105374660 : Intron Variant | AD |
rs7721685 | chr5:13399522 | A>G | SNV | LOC105374660 : Intron Variant | AD |
rs734826 | chr16:13396523 | A>C | SNV | SHISA9 : Intron Variant | AD |
rs985765 | chr5:13394059 | G>A | SNV | Intergenic | AD |
rs1037112 | chr5:13373983 | A>G | SNV | Intergenic | AD |
rs8076501 | chr17:13291872 | G>A | SNV | Intergenic | AD |
rs357159 | chr3:13267240 | G>C | SNV | IQSEC1 : Intron Variant | AD |
rs10832000 | chr11:13228852 | A>G | SNV | Intergenic | AD |
rs7108752 | chr11:13218012 | A>G | SNV | Intergenic | AD |
rs7112005 | chr11:13217953 | T>C | SNV | Intergenic | AD |
rs11022710 | chr11:13216162 | T>C | SNV | Intergenic | AD |
rs2674959 | chr17:13211937 | G>T | SNV | Intergenic | AD |
rs503506 | chr4:13147498 | G>A | SNV | LOC105374494 : Intron Variant | AD |
rs1501304 | chr16:13050831 | T>A / T>C | SNV | SHISA9 : Intron Variant | AD |
rs360534 | chr20:13007876 | G>A | SNV | SPTLC3 : 2KB Upstream Variant | AD |
rs17237639 | chr5:12975822 | A>G / A>T | SNV | LOC105374658 : Intron Variant | AD |
rs1017454 | chr5:12975210 | G>A | SNV | LOC105374658 : Intron Variant | AD |
rs9680021 | chr20:12917973 | A>C | SNV | LOC101929486 : Intron Variant | AD |
rs10831916 | chr11:12889689 | C>T | SNV | TEAD1 : Intron Variant | AD |
rs10809838 | chr9:12766338 | T>G | SNV | LURAP1L-AS1 : Intron Variant | AD |
rs9871587 | chr3:12755508 | G>A | SNV | TMEM40 : Intron Variant | AD |
rs11055041 | chr12:12750648 | T>A | SNV | APOLD1 : Intron Variant | AD |
rs17616845 | chr7:12741918 | T>C | SNV | Intergenic | AD |
rs13064447 | chr3:12711632 | C>A | SNV | Intergenic | AD |
rs11694463 | chr2:12641495 | T>C | SNV | Intergenic | ND |
rs6432321 | chr2:12638219 | T>C | SNV | Intergenic | AD |
rs3010931 | chr1:12624318 | C>T | SNV | Intergenic | AD |
rs12708762 | chr16:12617108 | C>A / C>G | SNV | Intergenic | CD |
rs13106 | chr3:12583081 | G>A | SNV | MKRN2 : 3 Prime UTR Variant | AD |
rs760943 | chr1:12538404 | T>C | SNV | Intergenic | AD |
rs2504899 | chr6:12531319 | G>T | SNV | Intergenic | AD |
rs73411566 | chr11:12433197 | T>C | SNV | PARVA : Intron Variant | OD |
rs4135275 | chr3:12402345 | A>G | SNV | PPARG : Intron Variant | AD |
rs4757381 | chr11:12347098 | G>A | SNV | MICALCL : Intron Variant | AD |
rs10831798 | chr11:12346259 | T>C | SNV | MICALCL : Intron Variant | AD |
rs9676962 | chr19:12330430 | C>T | SNV | ZNF563 : Intron Variant | AD |
rs1593000 | chr19:12329054 | C>T | SNV | ZNF563 : Intron Variant | AD |
rs12610507 | chr19:12325596 | A>C | SNV | ZNF563 : Intron Variant | AD |
rs7246738 | chr19:12324088 | T>C | SNV | ZNF563 : Intron Variant | AD |
rs7256140 | chr19:12299109 | G>T | SNV | Intergenic | AD |
rs17627328 | chr17:12284988 | G>A / G>C | SNV | Intergenic | ND |
rs17175889 | chr9:12206873 | T>G | SNV | Intergenic | ND |
rs12307111 | chr12:12205590 | C>A | SNV | LRP6 : Intron Variant | AD |
rs10831759 | chr11:12199835 | A>G | SNV | MICAL2 : Intron Variant | ND |
rs17477949 | chr11:12197656 | C>T | SNV | MICAL2 : Intron Variant | ND |
rs350255 | chr16:12111685 | A>G | SNV | SNX29 : Intron Variant | AD |
rs183008 | chr16:12107834 | T>C | SNV | SNX29 : Intron Variant | AD |
rs350212 | chr16:12060521 | A>G | SNV | SNX29 : Intron Variant | AD |
rs1570989 | chr6:12048594 | A>G | SNV | HIVEP1 : Intron Variant | AD | ND |
rs12582693 | chr12:11993007 | G>T | SNV | Intergenic | ND |
rs1036668 | chr2:11992512 | G>T | SNV | Intergenic | AD |
rs9657521 | chr8:11972993 | A>C / A>T | SNV | Intergenic | AD |
rs1787984 | chr18:11972440 | A>G | SNV | Intergenic | AD |
rs619671 | chr18:11961190 | C>T | SNV | Intergenic | AD |
rs663749 | chr18:11957686 | G>C | SNV | Intergenic | AD |
rs2961557 | chr12:11956571 | A>C / A>T | SNV | Intergenic | AD |
rs2448038 | chr12:11950371 | A>G | SNV | Intergenic | AD |
rs6777876 | chr3:11915124 | A>G | SNV | Intergenic | AD |
rs11804222 | chr1:11876457 | G>A | SNV | Intergenic | AD |
rs154148 | chr16:11862621 | T>C | SNV | LOC105371084 : Intron Variant | AD |
rs804292 | chr8:11786406 | G>A | SNV | NEIL2 : 3 Prime UTR Variant | AD | ND |
rs10864540 | chr1:11778042 | A>G | SNV | C1orf167 : Intron Variant LOC102724659 : Non Coding Transcript Variant | ND |
rs874651 | chr11:11757827 | C>T | SNV | Intergenic | AD |
rs4750099 | chr10:11753576 | G>A / G>T | SNV | ECHDC3 : Intron Variant | AD |
rs8043748 | chr16:11752375 | A>G | SNV | ZC3H7A : Intron Variant | AD |
rs75433892 | chr18:11712923 | G>A | SNV | GNAL : Intron Variant | AD |
rs999700 | chrX:11699179 | T>C | SNV | Intergenic | AD |
rs205534 | chr12:11688183 | A>G | SNV | ETV6 : Intron Variant | AD |
rs2526100 | chr7:11638151 | T>C | SNV | THSD7A : Intron Variant | AD |
rs7562399 | chr2:11627156 | G>A | SNV | GREB1 : Intron Variant | AD |
rs12476319 | chr2:11608280 | T>C | SNV | GREB1 : Intron Variant | AD |
rs1478892 | chr8:11591020 | G>T | SNV | Intergenic | AD |
rs11646835 | chr16:11519313 | G>A | SNV | LOC400499 : Intron Variant | AD |
rs6927244 | chr6:11510625 | G>A | SNV | LOC105374928 : Intron Variant | AD |
rs12222290 | chr11:11455298 | A>G | SNV | GALNT18 : Intron Variant | AD |
rs12932948 | chr16:11450817 | G>A | SNV | LOC400499 : Missense Variant | AD |
rs12932782 | chr16:11450014 | C>T | SNV | LOC400499 : Intron Variant | AD |
rs4310165 | chr8:11437066 | C>A / C>T | SNV | FAM167A : Intron Variant FAM167A-AS1 : Intron Variant | AD |
rs10044218 | chr5:11412934 | A>G | SNV | CTNND2 : Intron Variant | ND |
rs2606742 | chr3:11350243 | G>A | SNV | ATG7 : Intron Variant | ND |
rs2594978 | chr3:11341873 | C>A | SNV | ATG7 : Intron Variant | ND |
rs2606747 | chr3:11333481 | T>C / T>G | SNV | ATG7 : Intron Variant | ND |
rs2594995 | chr3:11327643 | G>A | SNV | ATG7 : Intron Variant | ND |
rs17383790 | chr4:11318787 | T>C | SNV | Intergenic | ND |
rs6869903 | chr5:11300742 | T>C | SNV | CTNND2 : Intron Variant | AD |
rs10253872 | chr7:11282266 | C>T | SNV | LOC105375153 : Intron Variant | AD |
rs4910291 | chr11:11268524 | G>A | SNV | Intergenic | AD |
rs11835196 | chr12:11258992 | C>T | SNV | LOC107987435 : Intron Variant | AD |
rs17699089 | chr19:11233119 | A>G | SNV | DOCK6 : Intron Variant | AD |
rs12463177 | chr19:11231004 | G>A / G>C | SNV | DOCK6 : Intron Variant | AD |
rs9366751 | chr6:11229264 | A>G | SNV | NEDD9 : Intron Variant | AD |
rs4804154 | chr19:11223503 | C>T | SNV | DOCK6 : Intron Variant | AD |
rs3810308 | chr19:11222920 | T>C | SNV | DOCK6 : Intron Variant | AD |
rs3826815 | chr19:11221829 | C>T | SNV | DOCK6 : Intron Variant | AD |
rs443137 | chr3:11212035 | G>A | SNV | HRH1 : Intron Variant LOC102723663 : Intron Variant | AD |
rs433303 | chr3:11203220 | C>G / C>T | SNV | HRH1 : Intron Variant LOC102723663 : Intron Variant | AD |
rs9822871 | chr3:11197680 | C>T | SNV | HRH1 : Intron Variant LOC102723663 : Intron Variant | AD |
rs4697674 | chr4:11131521 | A>G | SNV | Intergenic | ND |
rs11121671 | chr1:10983723 | C>A / C>T | SNV | C1orf127 : 2KB Upstream Variant | AD |
rs10052295 | chr5:10977210 | A>G | SNV | CTNND2 : Intron Variant LOC105374654 : Intron Variant | OD |
rs12112329 | chr7:10968838 | T>C | SNV | LOC107986767 : 500B Downstream Variant | AD |
rs1681300 | chr7:10950685 | G>A | SNV | LOC107986767 : Intron Variant | AD |
rs3774084 | chr3:10916591 | T>C | SNV | SLC6A11 : Intron Variant LOC105376950 : Intron Variant | AD |
rs4713039 | chr6:10906023 | A>G | SNV | SYCP2L : Synonymous Variant | AD |
rs1995364 | chr5:10903669 | A>G | SNV | Intergenic | AD |
rs2409665 | chr8:10878723 | G>C | SNV | Intergenic | ND |
rs2024683 | chr20:10863192 | A>G | SNV | C20orf187 : Non Coding Transcript Variant | AD |
rs2890930 | chr9:10861806 | A>C / A>G | SNV | Intergenic | ND |
rs4398608 | chr5:10847858 | G>T | SNV | Intergenic | AD |
rs2918406 | chr5:10829507 | A>C | SNV | Intergenic | AD |
rs9312745 | chr5:10827578 | A>G | SNV | Intergenic | AD |
rs6554603 | chr5:10819173 | T>C | SNV | Intergenic | AD |
rs7725091 | chr5:10810492 | C>T | SNV | Intergenic | AD |
rs6882716 | chr5:10797774 | G>A | SNV | Intergenic | AD |
rs10845212 | chr12:10773758 | C>T | SNV | LOC101928162 : Intron Variant | AD |
rs10738186 | chr9:10753414 | G>A | SNV | Intergenic | OD |
rs4780986 | chr16:10721373 | A>G | SNV | TEKT5 : Intron Variant | AD |
rs61776326 | chr1:10682063 | G>A | SNV | CASZ1 : Intron Variant | AD |
rs11121604 | chr1:10669945 | A>C / A>G | SNV | CASZ1 : Intron Variant | AD |
rs284320 | chr1:10666963 | T>C | SNV | CASZ1 : Intron Variant | AD |
rs284322 | chr1:10665441 | G>A / G>T | SNV | CASZ1 : Missense Variant | AD |
rs7267595 | chr20:10663202 | A>C / A>T | SNV | JAG1 : Intron Variant | AD |
rs476164 | chr1:10659509 | T>A / T>C | SNV | CASZ1 : Intron Variant | AD |
rs2242287 | chr1:10654854 | T>C | SNV | CASZ1 : Intron Variant | AD |
rs284295 | chr1:10652040 | A>G | SNV | CASZ1 : Intron Variant | AD |
rs284296 | chr1:10652032 | A>G | SNV | CASZ1 : Intron Variant | AD |
rs284298 | chr1:10650198 | G>A | SNV | CASZ1 : Intron Variant | AD |
rs284300 | chr1:10649252 | C>A / C>G / C>T | SNV | CASZ1 : Intron Variant | AD |
rs778228 | chr1:10648085 | A>G | SNV | CASZ1 : Synonymous Variant | AD |
rs284243 | chr1:10645823 | A>G | SNV | CASZ1 : Intron Variant | AD |
rs61776290 | chr1:10634850 | C>T | SNV | Intergenic | AD |
rs284301 | chr1:10634068 | G>A | SNV | Intergenic | AD |
rs284303 | chr1:10630826 | C>T | SNV | PEX14 : 500B Downstream Variant | AD |
rs185864 | chr1:10627669 | G>C | SNV | PEX14 : Intron Variant | AD |
rs190775 | chr1:10623626 | G>T | SNV | PEX14 : Intron Variant | AD |
rs284235 | chr1:10618786 | C>T | SNV | PEX14 : Intron Variant | AD |
rs284237 | chr1:10618553 | G>A | SNV | PEX14 : Intron Variant | AD |
rs284238 | chr1:10618431 | A>T | SNV | PEX14 : Intron Variant | AD |
rs3790630 | chr1:10613037 | C>T | SNV | PEX14 : Intron Variant | AD |
rs6666075 | chr1:10609041 | C>G | SNV | PEX14 : Intron Variant | AD |
rs12722934 | chr1:10608322 | A>T | SNV | PEX14 : Intron Variant | AD |
rs6913109 | chr6:10607699 | T>C | SNV | GCNT2 : Intron Variant | AD |
rs11121599 | chr1:10606678 | A>G | SNV | PEX14 : Intron Variant | AD |
rs9822272 | chr3:10600838 | A>G | SNV | ATP2B2 : Intron Variant | AD |
rs11121598 | chr1:10598145 | G>A | SNV | PEX14 : Intron Variant | AD |
rs10864468 | chr1:10595652 | G>A | SNV | PEX14 : Intron Variant | AD |
rs2540275 | chr2:10527623 | G>A | SNV | Intergenic | AD |
rs10488945 | chr4:10488654 | T>G | SNV | LOC105374482 : Non Coding Transcript Variant | AD |
rs470790 | chr6:10460327 | T>C | SNV | Intergenic | AD |
rs765805 | chr7:10429907 | C>T | SNV | Intergenic | AD |
rs1111644 | chr7:10412949 | T>G | SNV | Intergenic | AD |
rs6786239 | chr3:10407088 | C>T | SNV | ATP2B2 : Intron Variant | CD |
rs2214261 | chrX:10337289 | G>A | SNV | Intergenic | AD |
rs4102739 | chr12:10327909 | A>G | SNV | KLRD1 : Intron Variant | AD |
rs4509385 | chr8:10322686 | A>G | SNV | MSRA : Intron Variant | ND |
rs10089263 | chr8:10318996 | A>T | SNV | MSRA : Intron Variant | ND |
rs999339 | chr17:10295614 | G>A | SNV | Intergenic | ND |
rs12388359 | chrX:10263651 | G>T | SNV | Intergenic | AD |
rs2475335 | chr9:10260263 | C>T | SNV | PTPRD : Intron Variant | AD |
rs2241312 | chr3:10259616 | A>G | SNV | TATDN2 : Intron Variant | AD |
rs11707074 | chr3:10250959 | C>T | SNV | TATDN2 : Intron Variant | AD |
rs4741020 | chr9:10247217 | T>C | SNV | PTPRD : Intron Variant | AD |
rs10225194 | chr7:10239179 | T>G | SNV | Intergenic | AD |
rs17527069 | chr10:10235382 | T>C | SNV | Intergenic | AD |
rs1097863 | chr16:10233472 | T>G | SNV | LOC105371078 : Intron Variant | AD |
rs7844115 | chr8:10206985 | C>G | SNV | MSRA : Intron Variant | ND |
rs6077681 | chr20:10173796 | T>C | SNV | SNAP25-AS1 : Intron Variant LOC105372524 : Intron Variant | AD |
rs11121524 | chr1:10172476 | C>G | SNV | UBE4B : Intron Variant | AD |
rs9949713 | chr18:10142326 | G>A / G>T | SNV | Intergenic | AD |
rs532241 | chr18:10140632 | T>G | SNV | Intergenic | AD |
rs906071 | chr5:10109273 | T>C | SNV | Intergenic | ND |
rs7206714 | chr16:10084138 | A>C | SNV | GRIN2A : Intron Variant | AD |
rs1896785 | chr5:9987622 | A>G | SNV | Intergenic | AD |
rs917174 | chr7:9961159 | A>G | SNV | LOC105375146 : Non Coding Transcript Variant | AD |
rs1035961 | chr5:9928750 | A>C | SNV | Intergenic | ND |
rs1557978 | chr7:9926280 | C>T | SNV | LOC105375147 : Intron Variant | AD |
rs13252510 | chr8:9908378 | G>A | SNV | Intergenic | AD |
rs11664080 | chr18:9888030 | C>A / C>T | SNV | TXNDC2 : Stop Gained | AD |
rs2915131 | chr7:9886401 | T>C | SNV | LOC105375147 : Intron Variant | AD |
rs2915125 | chr7:9867081 | T>C | SNV | LOC105375147 : Intron Variant | AD |
rs728260 | chr7:9863728 | G>A | SNV | LOC105375147 : Intron Variant | AD |
rs2209192 | chr9:9862171 | C>G | SNV | PTPRD : Intron Variant | AD |
rs12920919 | chr16:9844123 | T>C | SNV | GRIN2A : Intron Variant | ND |
rs1933734 | chr1:9842070 | T>C | SNV | Intergenic | AD |
rs424508 | chr17:9749551 | T>C | SNV | Intergenic | AD |
rs4128324 | chr8:9651369 | A>G | SNV | TNKS : Intron Variant | AD |
rs855250 | chr6:9608654 | A>C | SNV | Intergenic | AD |
rs930076 | chr5:9550530 | T>C | SNV | SNHG18 : 500B Downstream Variant | AD |
rs17362650 | chr2:9536284 | T>C | SNV | ADAM17 : Intron Variant | AD |
rs7216753 | chr17:9446509 | A>C | SNV | STX8 : Intron Variant | AD |
rs11922615 | chr3:9416623 | A>G | SNV | SETD5 : Intron Variant | AD |
rs4509227 | chr7:9407710 | T>A / T>C | SNV | Intergenic | AD |
rs6443238 | chr3:9407371 | C>T | SNV | SETD5 : Intron Variant | AD |
rs268487 | chr5:9403862 | A>G | SNV | SEMA5A : Intron Variant | AD |
rs1805243 | chr5:9379998 | T>C / T>G | SNV | SEMA5A : 5 Prime UTR Variant | AD |
rs7772742 | chr6:9314121 | G>A | SNV | Intergenic | AD |
rs4684630 | chr3:9245460 | C>A | SNV | SRGAP3 : Intron Variant | ND |
rs17530358 | chr3:9158691 | G>A | SNV | SRGAP3 : Intron Variant | AD |
rs3743832 | chr16:9120023 | A>C | SNV | C16orf72 : 500B Downstream Variant | AD |
rs7296295 | chr12:8986686 | G>A | SNV | Intergenic | AD |
rs827628 | chr10:8978271 | T>C | SNV | Intergenic | AD |
rs6959898 | chr7:8970692 | A>G | SNV | Intergenic | AD |
rs2206266 | chr20:8968417 | T>C | SNV | LOC105372522 : Non Coding Transcript Variant | AD |
rs12091891 | chr1:8940161 | A>G | SNV | Intergenic | AD |
rs373204 | chr8:8913892 | T>C | SNV | ERI1 : Intron Variant | ND |
rs12002381 | chr9:8870553 | C>T | SNV | PTPRD : Intron Variant | AD |
rs10412487 | chr19:8862541 | T>C | SNV | MUC16 : Intron Variant | AD |
rs2117099 | chr9:8847233 | G>A | SNV | PTPRD : Intron Variant | AD |
rs17049541 | chr3:8778715 | G>A | SNV | Intergenic | AD |
rs237899 | chr3:8766829 | G>A / G>C | SNV | OXTR : Intron Variant | AD |
rs994247 | chr7:8760938 | C>T | SNV | Intergenic | ND |
rs1273396 | chr16:8722955 | C>G | SNV | ABAT : Intron Variant | ND |
rs7782816 | chr7:8700732 | C>T | SNV | NXPH1 : Intron Variant | AD |
rs10840110 | chr11:8682544 | C>T | SNV | TRIM66 : Intron Variant RPL27A : 5 Prime UTR Variant SNORA3A : 2KB Upstream Variant | AD |
rs10505737 | chr12:8651976 | C>A | SNV | MFAP5 : Intron Variant | AD |
rs7208821 | chr17:8573425 | C>T | SNV | MYH10 : Intron Variant | AD |
rs7026937 | chr9:8558331 | G>A / G>C | SNV | PTPRD : Intron Variant | AD |
rs8061765 | chr16:8540871 | G>A | SNV | TMEM114 : Intron Variant | AD |
rs11777086 | chr8:8526969 | G>T | SNV | Intergenic | AD |
rs2921010 | chr8:8372845 | G>A | SNV | SGK223 : Intron Variant | ND |
rs12001948 | chr9:8320837 | G>C | SNV | PTPRD : Intron Variant | ND |
rs6133573 | chr20:8311010 | T>C | SNV | PLCB1 : Intron Variant | AD |
rs2945891 | chr8:8297953 | G>A | SNV | Intergenic | AD |
rs7797010 | chr7:8290132 | G>T | SNV | LOC100505938 : Intron Variant | AD |
rs2719791 | chr20:8287092 | C>T | SNV | PLCB1 : Intron Variant | ND |
rs204926 | chr11:8233559 | G>A | SNV | LMO1 : Intron Variant LOC105376536 : Non Coding Transcript Variant | AD |
rs12574271 | chr11:8232956 | G>T | SNV | LMO1 : Intron Variant LOC105376536 : Non Coding Transcript Variant | AD |
rs110420 | chr11:8231502 | T>C | SNV | LMO1 : Intron Variant LOC105376536 : Non Coding Transcript Variant | AD |
rs11041820 | chr11:8229891 | G>A | SNV | LMO1 : Intron Variant LOC105376536 : Non Coding Transcript Variant | AD |
rs4758317 | chr11:8229264 | C>A | SNV | LMO1 : Intron Variant LOC105376536 : 2KB Upstream Variant | AD |
rs6086371 | chr20:8229070 | C>T | SNV | PLCB1 : Intron Variant | ND |
rs2290450 | chr11:8226935 | C>T | SNV | LMO1 : Non Coding Transcript Variant | AD |
rs2290451 | chr11:8226893 | C>A / C>G | SNV | LMO1 : Non Coding Transcript Variant | AD |
rs1781276 | chr9:8206576 | C>T | SNV | Intergenic | AD |
rs4883071 | chr12:8118506 | A>G | SNV | CLEC4A : Intron Variant | AD |
rs10411526 | chr19:8107797 | A>G | SNV | FBN3 : Intron Variant | AD |
rs1406095 | chr11:8073135 | T>C | SNV | TUB : Intron Variant | ND |
rs12943817 | chr17:8071516 | C>T | SNV | Intergenic | AD |
rs3782683 | chr12:8039315 | C>A / C>T | SNV | FOXJ2 : Intron Variant | AD |
rs6039005 | chr20:8025549 | G>A / G>T | SNV | LOC105372520 : Intron Variant | AD |
rs7503918 | chr17:8018707 | C>T | SNV | GUCY2D : Intron Variant | AD |
rs7942511 | chr11:7940384 | A>G | SNV | OR10A3 : 2KB Upstream Variant | AD |
rs11041680 | chr11:7940250 | G>A | SNV | OR10A3 : 2KB Upstream Variant | AD |
rs11041679 | chr11:7940205 | C>A / C>T | SNV | OR10A3 : 2KB Upstream Variant | AD |
rs4758259 | chr11:7939583 | C>T | SNV | OR10A3 : 2KB Upstream Variant | AD |
rs1397598 | chr11:7937281 | A>G | SNV | Intergenic | AD |
rs7779286 | chr7:7936612 | A>G | SNV | LOC107986765 : Intron Variant | AD |
rs10839947 | chr11:7936406 | G>A | SNV | Intergenic | AD |
rs2041567 | chr7:7932706 | T>C | SNV | LOC107986765 : Intron Variant | AD |
rs3930459 | chr11:7932411 | T>C | SNV | Intergenic | AD |
rs10839942 | chr11:7932003 | C>A | SNV | Intergenic | AD |
rs11041670 | chr11:7931373 | T>G | SNV | Intergenic | AD |
rs7928451 | chr11:7928313 | G>A | SNV | OR10A6 : Missense Variant | AD |
rs7933807 | chr11:7928244 | A>C | SNV | OR10A6 : Missense Variant | AD |
rs10769847 | chr11:7901104 | T>C | SNV | LOC283299 : Intron Variant | AD |
rs17315616 | chr11:7892393 | T>C | SNV | LOC283299 : Intron Variant | AD |
rs17315588 | chr11:7892364 | C>A | SNV | LOC283299 : Intron Variant | AD |
rs10047605 | chr12:7870680 | G>T | SNV | SLC2A14 : Intron Variant | AD |
rs11612319 | chr12:7864329 | G>A | SNV | SLC2A14 : Intron Variant | AD |
rs1894829 | chr12:7861445 | A>G | SNV | SLC2A14 : Intron Variant | AD |
rs7965203 | chr12:7847740 | T>G | SNV | SLC2A14 : Intron Variant | AD |
rs11056079 | chr12:7844294 | C>T | SNV | SLC2A14 : Intron Variant | AD |
rs117253780 | chr20:7822573 | C>T | SNV | Intergenic | ND |
rs8058542 | chr16:7804982 | G>A | SNV | Intergenic | AD |
rs12597282 | chr16:7794410 | T>C | SNV | Intergenic | AD |
rs3862445 | chr16:7792520 | T>C | SNV | Intergenic | AD |
rs10125984 | chr9:7786701 | C>T | SNV | Intergenic | AD |
rs3745376 | chr19:7768804 | G>T | SNV | CLEC4M : Intron Variant LOC105372263 : 2KB Upstream Variant | AD |
rs12453814 | chr17:7761975 | A>G | SNV | DNAH2 : Intron Variant | AD |
rs2024372 | chr7:7743288 | G>A | SNV | UMAD1 : Intron Variant | AD |
rs10486187 | chr7:7739693 | T>C | SNV | UMAD1 : Intron Variant | AD |
rs13237260 | chr7:7739460 | G>T | SNV | UMAD1 : Intron Variant | AD |
rs4720751 | chr7:7729732 | G>A | SNV | UMAD1 : Intron Variant | AD |
rs9927040 | chr16:7716853 | T>G | SNV | Intergenic | ND |
rs10264890 | chr7:7680356 | T>G | SNV | RPA3 : Intron Variant UMAD1 : Intron Variant | AD |
rs1557997 | chr7:7664329 | G>A | SNV | RPA3 : Intron Variant UMAD1 : Intron Variant | AD |
rs9502630 | chr6:7633425 | G>A | SNV | Intergenic | AD |
rs12527897 | chr6:7632010 | A>G | SNV | Intergenic | AD |
rs4472926 | chr11:7592118 | A>G | SNV | PPFIBP2 : Intron Variant LOC105376535 : 2KB Upstream Variant | AD |
rs4742378 | chr9:7578222 | C>T | SNV | Intergenic | AD |
rs6578882 | chr11:7578160 | C>A | SNV | PPFIBP2 : Intron Variant LOC105376535 : Intron Variant | ND |
rs12247601 | chr10:7569535 | T>C | SNV | ITIH5 : Intron Variant | AD |
rs2381642 | chr9:7563692 | A>G | SNV | Intergenic | AD |
rs1485179 | chr3:7562021 | C>T | SNV | GRM7 : Intron Variant | AD |
rs1507030 | chr16:7561154 | C>G | SNV | RBFOX1 : Intron Variant | ND |
rs576192 | chr18:7519003 | T>A / T>G | SNV | Intergenic | ND |
rs533682 | chr18:7491480 | T>C | SNV | Intergenic | ND |
rs567338 | chr18:7488972 | G>A | SNV | Intergenic | ND |
rs12805648 | chr11:7488335 | A>T | SNV | OLFML1 : Missense Variant | ND |
rs2287919 | chr19:7464529 | C>T | SNV | ARHGEF18 : Intron Variant | AD |
rs1868616 | chr3:7463800 | A>G | SNV | GRM7 : Intron Variant | ND |
rs12610760 | chr19:7451357 | A>G | SNV | ARHGEF18 : Intron Variant | AD |
rs7248066 | chr19:7445470 | G>A | SNV | ARHGEF18 : Intron Variant | AD |
rs75562159 | chr1:7444081 | C>A / C>T | SNV | CAMTA1 : Intron Variant LOC101928836 : 2KB Upstream Variant | AD |
rs7077972 | chr10:7438730 | A>C | SNV | Intergenic | AD |
rs977749 | chr11:7363180 | T>C | SNV | SYT9 : Intron Variant | AD |
rs10489142 | chr1:7303250 | A>G | SNV | CAMTA1 : Intron Variant | AD |
rs4797283 | chr18:7249742 | C>T | SNV | LOC105371973 : Intron Variant | AD |
rs9392863 | chr6:7194776 | G>A | SNV | RREB1 : Intron Variant | AD |
rs12947697 | chr17:7186298 | C>T | SNV | Intergenic | AD |
rs10500204 | chr19:7182952 | A>C | SNV | INSR : Intron Variant | AD |
rs34870220 | chr17:7181592 | C>T | SNV | Intergenic | AD |
rs11641647 | chr16:7144839 | A>G | SNV | RBFOX1 : Intron Variant | AD |
rs1904224 | chr16:7141865 | A>T | SNV | RBFOX1 : Intron Variant | AD |
rs922471 | chr16:7140896 | G>C / G>T | SNV | RBFOX1 : Intron Variant | AD |
rs4444357 | chr16:7140074 | C>G / C>T | SNV | RBFOX1 : Intron Variant | AD |
rs11863081 | chr16:7139575 | A>C | SNV | RBFOX1 : Intron Variant | AD |
rs35269146 | chr16:7139413 | T>A | SNV | RBFOX1 : Intron Variant | AD |
rs8047522 | chr16:7139410 | T>C | SNV | RBFOX1 : Intron Variant | AD |
rs8052094 | chr16:7138545 | T>C / T>G | SNV | RBFOX1 : Intron Variant | AD |
rs6500918 | chr16:7136901 | G>T | SNV | RBFOX1 : Intron Variant | AD |
rs1871256 | chr16:7130063 | A>G | SNV | RBFOX1 : Intron Variant | AD |
rs11077139 | chr16:7124873 | C>A / C>G | SNV | RBFOX1 : Intron Variant | AD |
rs6970410 | chr7:7116841 | C>T | SNV | Intergenic | AD |
rs1864193 | chr19:7114202 | C>A | SNV | INSR : 3 Prime UTR Variant | AD |
rs35569480 | chr16:7105447 | A>G | SNV | RBFOX1 : Intron Variant | AD |
rs7034275 | chr9:7067344 | G>C | SNV | KDM4C : Intron Variant | ND |
rs6936076 | chr6:7063038 | G>A | SNV | Intergenic | AD |
rs1407862 | chr9:7032776 | G>A | SNV | KDM4C : Intron Variant | AD |
rs10758821 | chr9:7030268 | G>T | SNV | KDM4C : Intron Variant | AD |
rs10975990 | chr9:7026716 | G>A | SNV | KDM4C : Intron Variant | AD |
rs4797265 | chr18:6928181 | G>A / G>C / G>T | SNV | LINC00668 : Non Coding Transcript Variant | AD |
rs459998 | chr19:6914519 | T>C | SNV | ADGRE1 : Intron Variant LOC105372256 : Intron Variant | CD |
rs673320 | chr19:6909554 | C>A | SNV | ADGRE1 : Intron Variant LOC105372256 : Intron Variant | AD |
rs186715 | chr19:6878125 | T>G | SNV | Intergenic | ND |
rs2567261 | chr18:6868926 | T>C | SNV | ARHGAP28 : Intron Variant | AD |
rs4807101 | chr19:6815937 | C>T | SNV | VAV1 : Intron Variant | AD |
rs11998950 | chr9:6811507 | C>T | SNV | KDM4C : Intron Variant | ND |
rs10503364 | chr8:6805802 | T>C | SNV | LOC107986909 : Non Coding Transcript Variant | ND |
rs6054517 | chr20:6790723 | C>A | SNV | Intergenic | AD |
rs17078124 | chr8:6779667 | C>T | SNV | Intergenic | AD |
rs2912089 | chr8:6777253 | G>A / G>C | SNV | Intergenic | AD |
rs2912091 | chr8:6776693 | C>A / C>T | SNV | Intergenic | AD |
rs17637986 | chr8:6776181 | T>G | SNV | Intergenic | AD |
rs1046449 | chr8:6758233 | G>A | SNV | AGPAT5 : 3 Prime UTR Variant | ND |
rs2980700 | chr8:6755315 | G>A | SNV | AGPAT5 : Intron Variant | AD |
rs2936512 | chr8:6741484 | T>C | SNV | AGPAT5 : Intron Variant | AD |
rs278020 | chr1:6704583 | C>T | SNV | Intergenic | AD |
rs10839595 | chr11:6698955 | G>A | SNV | Intergenic | AD |
rs28620095 | chr4:6673802 | A>G | SNV | LOC105374366 : Non Coding Transcript Variant LOC93622 : 2KB Upstream Variant | AD |
rs10779795 | chr1:6617004 | A>G | SNV | PHF13 : Intron Variant | AD |
rs731024 | chr1:6584663 | G>A | SNV | ZBTB48 : Intron Variant | AD |
rs2442623 | chr8:6518817 | G>A | SNV | MCPH1 : Intron Variant ANGPT2 : Intron Variant | ND |
rs3020213 | chr8:6512409 | C>T | SNV | MCPH1 : Intron Variant ANGPT2 : Intron Variant | ND |
rs6117294 | chr20:6490158 | T>G | SNV | CASC20 : Intron Variant | AD |
rs1970008 | chr20:6487724 | A>G | SNV | CASC20 : Intron Variant | AD |
rs10485705 | chr20:6487614 | G>T | SNV | CASC20 : Intron Variant | AD |
rs12932935 | chr16:6475759 | T>G | SNV | RBFOX1 : Intron Variant | CD |
rs6506389 | chr18:6467157 | C>T | SNV | Intergenic | AD |
rs7018378 | chr8:6420991 | G>A | SNV | MCPH1 : Intron Variant | ND |
rs6726264 | chr2:6411741 | T>C | SNV | LOC105373402 : Intron Variant | AD |
rs6723180 | chr2:6411725 | A>G | SNV | LOC105373402 : Intron Variant | AD |
rs1564032 | chr2:6389372 | T>C | SNV | Intergenic | AD |
rs6739653 | chr2:6382201 | G>A | SNV | Intergenic | AD |
rs2101469 | chr11:6376106 | T>C | SNV | Intergenic | AD |
rs10040610 | chr5:6353702 | T>C | SNV | LOC105374638 : Non Coding Transcript Variant | AD |
rs4345283 | chr5:6325737 | A>C | SNV | FLJ33360 : Intron Variant | AD |
rs12716179 | chr5:6317193 | T>C | SNV | FLJ33360 : Intron Variant | AD |
rs4758405 | chr11:6303404 | G>A / G>T | SNV | Intergenic | ND |
rs12531066 | chr7:6286516 | A>G | SNV | Intergenic | AD |
rs4724793 | chr7:6275135 | T>C | SNV | Intergenic | AD |
rs2185691 | chr10:6250644 | T>C | SNV | PFKFB3 : Intron Variant | AD |
rs2295435 | chr20:6116048 | C>T | SNV | FERMT1 : Intron Variant | CD |
rs1852319 | chr2:6112453 | A>G | SNV | Intergenic | AD |
rs12667392 | chr7:6112051 | A>C | SNV | USP42 : Intron Variant | ND |
rs2249724 | chr2:6095076 | A>C | SNV | Intergenic | AD |
rs2693871 | chr2:6093997 | A>G | SNV | Intergenic | AD |
rs17192650 | chr16:6066395 | G>A | SNV | RBFOX1 : Intron Variant | AD |
rs2693818 | chr2:6064376 | C>T | SNV | Intergenic | AD |
rs4749926 | chr10:6043349 | G>A | SNV | IL2RA : Intron Variant | ND |
rs216318 | chr12:6030095 | A>C | SNV | VWF : Intron Variant | AD |
rs1800385 | chr12:6018725 | C>A | SNV | VWF : Missense Variant | AD |
rs1993912 | chr9:5987781 | A>C | SNV | KIAA2026 : Intron Variant | AD |
rs917857 | chr12:5972658 | G>A | SNV | VWF : Intron Variant | CD |
rs6446414 | chr4:5962618 | T>A / T>C | SNV | C4orf50 : Intron Variant | AD |
rs7682973 | chr4:5943379 | A>G | SNV | C4orf50 : Intron Variant | AD |
rs4689294 | chr4:5917982 | G>A | SNV | C4orf50 : Intron Variant | AD |
rs7129741 | chr11:5902831 | A>G | SNV | Intergenic | AD |
rs4601752 | chr11:5902067 | A>G | SNV | Intergenic | AD |
rs7106300 | chr11:5901477 | C>T | SNV | Intergenic | AD |
rs17138815 | chr16:5901423 | C>T | SNV | RBFOX1 : Intron Variant | AD |
rs7654446 | chr4:5837110 | G>A / G>C | SNV | CRMP1 : Intron Variant | AD |
rs9661578 | chr1:5821692 | C>T | SNV | Intergenic | CD |
rs7813894 | chr8:5783921 | C>T | SNV | Intergenic | AD |
rs17028719 | chr1:5734948 | A>G | SNV | Intergenic | AD | ND |
rs11874707 | chr18:5731841 | G>T | SNV | Intergenic | AD |
rs2527128 | chr8:5726852 | C>A | SNV | Intergenic | AD |
rs2733022 | chr8:5724652 | T>C | SNV | Intergenic | AD |
rs2733020 | chr8:5724168 | A>C / A>T | SNV | Intergenic | AD |
rs2725730 | chr8:5724130 | A>C / A>G | SNV | Intergenic | AD |
rs1512791 | chr8:5723239 | A>C / A>G | SNV | Intergenic | AD |
rs263328 | chr8:5722353 | T>G | SNV | Intergenic | AD |
rs11948250 | chr5:5704121 | G>A | SNV | Intergenic | AD |
rs11950687 | chr5:5689233 | T>G | SNV | LOC105374634 : Intron Variant | AD |
rs852519 | chr7:5656494 | C>A / C>G / C>T | SNV | RNF216 : Intron Variant | AD |
rs10484314 | chr6:5647854 | A>G | SNV | FARS2 : Intron Variant | AD |
rs11256831 | chr10:5647095 | G>T | SNV | ASB13 : Intron Variant | AD |
rs4807045 | chr19:5621914 | T>C | SNV | SAFB2 : Intron Variant SAFB : 2KB Upstream Variant | AD |
rs10221410 | chr18:5605990 | C>T | SNV | EPB41L3 : Intron Variant LOC100286986 : Intron Variant | AD |
rs9328308 | chr6:5513258 | T>C | SNV | FARS2 : Intron Variant | AD |
rs366533 | chr11:5496255 | G>A | SNV | OR51B5 : Intron Variant | ND |
rs4074967 | chr12:5491300 | T>C / T>G | SNV | NTF3 : Intron Variant | AD |
rs8111234 | chr19:5426438 | T>C | SNV | Intergenic | AD |
rs11667049 | chr19:5421951 | A>G | SNV | Intergenic | AD |
rs3824435 | chr9:5377115 | C>T | SNV | PLGRKT : Intron Variant | AD |
rs9423407 | chr10:5313749 | C>T | SNV | Intergenic | AD |
rs7076488 | chr10:5291045 | G>A | SNV | Intergenic | AD |
rs9423593 | chr10:5290386 | C>T | SNV | Intergenic | AD |
rs2398236 | chr10:5289196 | A>G | SNV | Intergenic | AD |
rs4807016 | chr19:5258479 | G>A | SNV | PTPRS : Intron Variant | AD |
rs4465222 | chr1:5250198 | T>C | SNV | Intergenic | AD |
rs677735 | chr1:5235116 | A>G | SNV | Intergenic | AD |
rs16840183 | chr1:5220442 | T>G | SNV | Intergenic | AD |
rs17219798 | chrX:5176299 | G>A / G>T | SNV | Intergenic | AD |
rs814778 | chr5:5125559 | A>G | SNV | Intergenic | AD |
rs860085 | chr5:5125220 | A>C | SNV | Intergenic | AD |
rs270184 | chr5:5124466 | C>T | SNV | Intergenic | AD |
rs270188 | chr5:5124036 | G>A / G>C | SNV | Intergenic | AD |
rs7944388 | chr11:5121441 | A>G | SNV | Intergenic | ND |
rs814782 | chr5:5120689 | A>G | SNV | Intergenic | AD |
rs814786 | chr5:5119528 | C>T | SNV | Intergenic | AD |
rs1092985 | chr5:5115396 | C>T | SNV | Intergenic | AD |
rs2275928 | chr10:5105717 | G>A | SNV | AKR1C3 : Intron Variant | AD |
rs6811343 | chr4:5080268 | G>A | SNV | STK32B : Intron Variant | ND |
rs11035102 | chr11:5008227 | A>C / A>G / A>T | SNV | Intergenic | AD |
rs10849182 | chr12:4965172 | G>A | SNV | Intergenic | AD |
rs16836497 | chr4:4950950 | T>C | SNV | LOC101928306 : Intron Variant | AD |
rs2397990 | chr10:4786911 | C>T | SNV | Intergenic | AD |
rs968433 | chr20:4761434 | C>G | SNV | Intergenic | AD |
rs1756871 | chr9:4758022 | G>A | SNV | Intergenic | AD |
rs1045280 | chr17:4719343 | C>T | SNV | ARRB2 : Synonymous Variant | AD |
rs1000579 | chr4:4717767 | A>G | SNV | Intergenic | AD |
rs3786047 | chr17:4711803 | A>G | SNV | ARRB2 : Intron Variant | AD |
rs7215300 | chr17:4705327 | T>C | SNV | PELP1 : 2KB Upstream Variant LOC101559451 : Non Coding Transcript Variant | AD |
rs7225717 | chr17:4704757 | A>G | SNV | PELP1 : 2KB Upstream Variant LOC101559451 : Intron Variant | AD |
rs4790689 | chr17:4701905 | A>C | SNV | PELP1 : Intron Variant | AD |
rs4790688 | chr17:4701773 | C>T | SNV | PELP1 : Intron Variant | AD |
rs4790687 | chr17:4701339 | A>G | SNV | PELP1 : Intron Variant | AD |
rs12451741 | chr17:4700735 | G>T | SNV | PELP1 : Intron Variant | AD |
rs11087653 | chr20:4698873 | G>A / G>T | SNV | PRNP : Intron Variant | AD |
rs906453 | chr17:4691670 | C>T | SNV | PELP1 : Intron Variant | AD |
rs11078523 | chr17:4619872 | T>C | SNV | LOC105371498 : Intron Variant | AD |
rs12682807 | chr9:4574022 | A>C | SNV | SPATA6L : Intron Variant SLC1A1 : Intron Variant | AD |
rs1670530 | chr2:4544651 | C>T | SNV | Intergenic | AD |
rs17812250 | chr9:4517894 | A>G | SNV | SLC1A1 : Intron Variant | AD |
rs10814995 | chr9:4505544 | A>C | SNV | SLC1A1 : Intron Variant | AD |
rs16992410 | chr19:4487809 | A>G | SNV | HDGFRP2 : Intron Variant | AD |
rs648196 | chr2:4469921 | G>T | SNV | Intergenic | AD |
rs6139415 | chr20:4398224 | A>G | SNV | Intergenic | AD |
rs3792686 | chr4:4391341 | T>C | SNV | NSG1 : Intron Variant | AD |
rs3908110 | chr2:4369251 | C>A / C>T | SNV | Intergenic | AD |
rs8115863 | chr20:4259862 | T>C | SNV | Intergenic | AD |
rs4813680 | chr20:4259770 | C>A | SNV | Intergenic | AD |
rs13259289 | chr8:4252510 | T>C | SNV | CSMD1 : Intron Variant | AD |
rs2916464 | chr4:4247893 | T>A / T>C | SNV | TMEM128 : Intron Variant | AD |
rs2916468 | chr4:4247573 | T>C | SNV | TMEM128 : Intron Variant | AD |
rs2980103 | chr4:4244013 | A>G | SNV | TMEM128 : Intron Variant | AD |
rs12132422 | chr1:4235244 | A>G | SNV | Intergenic | AD |
rs12348139 | chr9:4232743 | T>C | SNV | GLIS3 : Intron Variant | ND |
rs3849840 | chr8:4212973 | C>A / C>T | SNV | CSMD1 : Intron Variant | AD |
rs17134615 | chr7:4209049 | T>C | SNV | SDK1 : Intron Variant | ND |
rs879151 | chr16:4200914 | C>A | SNV | SRL : Intron Variant | AD |
rs7797803 | chr7:4181432 | A>G | SNV | SDK1 : Intron Variant | ND |
rs1982176 | chr17:4171101 | A>C | SNV | ANKFY1 : Intron Variant | AD |
rs7851070 | chr9:4170457 | A>G | SNV | GLIS3 : Intron Variant | ND |
rs619672 | chr7:4156356 | G>A | SNV | SDK1 : Intron Variant | ND |
rs6037767 | chr20:4119674 | T>C | SNV | Intergenic | AD |
rs9927767 | chr16:4118169 | T>A | SNV | ADCY9 : 2KB Upstream Variant | AD |
rs11783062 | chr8:4089803 | T>C / T>G | SNV | CSMD1 : Intron Variant | AD |
rs10775349 | chr16:4029822 | G>C | SNV | ADCY9 : Intron Variant | AD |
rs1372631 | chr18:4026587 | T>G | SNV | DLGAP1 : Intron Variant | ND |
rs11978979 | chr7:3986377 | A>T | SNV | SDK1 : Intron Variant | AD |
rs745414 | chr19:3974967 | G>A | SNV | Intergenic | AD |
rs3957336 | chrX:3963903 | G>C | SNV | Intergenic | AD |
rs10848958 | chr12:3921938 | C>T | SNV | LOC105369608 : Non Coding Transcript Variant | AD |
rs3910707 | chr18:3873447 | A>C | SNV | DLGAP1 : Intron Variant | AD |
rs2930357 | chr8:3852138 | T>C / T>G | SNV | CSMD1 : Intron Variant | ND |
rs6084496 | chr20:3849815 | C>T | SNV | MAVS : Intron Variant | ND |
rs1451724 | chr11:3835438 | G>A | SNV | RHOG : Intron Variant | AD |
rs1451722 | chr11:3835323 | C>T | SNV | RHOG : Intron Variant | AD |
rs7545274 | chr1:3827697 | C>A | SNV | CEP104 : Intron Variant | AD |
rs7830364 | chr8:3824501 | A>G / A>T | SNV | CSMD1 : Intron Variant | AD |
rs11774223 | chr8:3809060 | C>T | SNV | CSMD1 : Intron Variant | ND |
rs1383951 | chr8:3785733 | C>T | SNV | CSMD1 : Intron Variant | AD |
rs9916609 | chr17:3769220 | C>A | SNV | ITGAE : Intron Variant | ND |
rs12678875 | chr8:3766524 | C>T | SNV | CSMD1 : Intron Variant | AD |
rs711548 | chr3:3752907 | A>G | SNV | LOC100130207 : Intron Variant | ND |
rs11062784 | chr12:3745301 | A>G | SNV | CRACR2A : Intron Variant | ND |
rs7100211 | chr10:3685755 | T>C | SNV | LOC105376360 : Intron Variant | ND |
rs871879 | chr5:3677068 | G>A | SNV | Intergenic | AD |
rs2672213 | chr11:3670187 | C>T | SNV | CHRNA10 : Intron Variant | AD |
rs7729527 | chr5:3616523 | T>A / T>C | SNV | LOC107986399 : Intron Variant | AD |
rs4959247 | chr6:3499729 | T>C | SNV | Intergenic | AD |
rs431220 | chr18:3467415 | C>T | SNV | GAPLINC : Intron Variant LOC105371965 : Intron Variant | AD |
rs7203180 | chr16:3420827 | C>T | SNV | Intergenic | AD |
rs16844280 | chr4:3407297 | C>T | SNV | RGS12 : Intron Variant | AD |
rs11732375 | chr4:3395236 | G>A | SNV | RGS12 : Intron Variant | AD |
rs10235080 | chr7:3379870 | A>G | SNV | SDK1 : Intron Variant | ND |
rs9503551 | chr6:3340483 | G>A | SNV | SLC22A23 : Intron Variant | ND |
rs2589293 | chr8:3339921 | C>G | SNV | CSMD1 : Intron Variant | ND |
rs12623730 | chr2:3330232 | C>T | SNV | TSSC1 : Intron Variant | ND |
rs6548153 | chr2:3322274 | C>A | SNV | TSSC1 : Intron Variant | ND |
rs1791124 | chr18:3316178 | T>G | SNV | Intergenic | AD |
rs9874556 | chr3:3314490 | A>G | SNV | LOC100130207 : Intron Variant | AD |
rs11251836 | chr10:3293255 | G>T | SNV | Intergenic | AD |
rs17135017 | chr10:3291338 | G>A | SNV | Intergenic | AD |
rs2005290 | chr17:3284718 | C>G | SNV | OR3A2 : Intron Variant | CD |
rs61751192 | chr18:3253944 | C>T | SNV | MYL12A : Synonymous Variant | CD |
rs13381416 | chr18:3251835 | A>G | SNV | MYL12A : Intron Variant | CD |
rs79794368 | chr18:3249131 | C>T | SNV | MYL12A : Intron Variant | CD |
rs10766825 | chr11:3244903 | T>C | SNV | Intergenic | AD |
rs10153321 | chr18:3176379 | G>A | SNV | MYOM1 : Intron Variant | ND |
rs7097793 | chr10:3144751 | G>C | SNV | PITRM1 : Intron Variant PITRM1-AS1 : Intron Variant | AD |
rs4468331 | chr11:3144182 | G>A | SNV | OSBPL5 : Intron Variant LOC107987158 : Intron Variant | AD |
rs597099 | chr5:3139044 | C>T | SNV | Intergenic | AD |
rs2306311 | chr10:3134197 | C>T | SNV | SNORD142 : Non Coding Transcript Variant PFKP : Intron Variant | AD |
rs4758533 | chr11:3128856 | A>G | SNV | OSBPL5 : Intron Variant | AD |
rs6578322 | chr11:3121800 | T>C | SNV | OSBPL5 : Intron Variant | AD |
rs1153459 | chr3:3116801 | T>C | SNV | Intergenic | AD |
rs4881084 | chr10:3108179 | G>A | SNV | PFKP : Intron Variant | AD |
rs7805247 | chr7:3070425 | C>T | SNV | Intergenic | ND |
rs10413635 | chr19:3068452 | C>T | SNV | LOC105372242 : Intron Variant | AD |
rs406598 | chr11:3055055 | G>A | SNV | CARS : Intron Variant | AD |
rs11768102 | chr7:3053663 | C>T | SNV | Intergenic | AD |
rs7805181 | chr7:3050648 | T>C | SNV | Intergenic | AD |
rs1004792 | chr16:3044260 | G>A | SNV | MMP25 : 2KB Upstream Variant | AD |
rs369461 | chr11:3040762 | T>C | SNV | CARS : Intron Variant | AD |
rs451041 | chr11:3039495 | A>C / A>G | SNV | CARS : Intron Variant | AD |
rs8125955 | chr20:3039311 | A>C | SNV | GNRH2 : 5 Prime UTR Variant | AD |
rs2798303 | chr4:3038860 | T>C | SNV | GRK4 : Intron Variant | AD |
rs1801058 | chr4:3037423 | T>C | SNV | GRK4 : Missense Variant | AD |
rs2857839 | chr4:3034903 | T>C | SNV | GRK4 : Intron Variant | AD |
rs434114 | chr11:3028980 | A>C / A>G | SNV | CARS : Intron Variant | AD |
rs2857845 | chr4:3026386 | A>T | SNV | GRK4 : Intron Variant | AD |
rs377765 | chr11:3025068 | C>G / C>T | SNV | CARS : Intron Variant | AD |
rs428726 | chr11:3024971 | G>A | SNV | CARS : Intron Variant | AD |
rs7481584 | chr11:3007859 | G>A | SNV | CARS : Intron Variant | AD |
rs729662 | chr11:3006910 | G>A | SNV | CARS : Synonymous Variant | AD |
rs596681 | chr8:3003080 | C>A / C>T | SNV | CSMD1 : Intron Variant LOC105377792 : Intron Variant | AD |
rs596215 | chr8:3002993 | A>G | SNV | CSMD1 : Intron Variant LOC105377792 : Intron Variant | AD |
rs12805661 | chr11:2999510 | C>T | SNV | Intergenic | AD |
rs4758621 | chr11:2988410 | A>G | SNV | NAP1L4 : Intron Variant | AD |
rs3814964 | chr11:2978277 | G>C / G>T | SNV | NAP1L4 : Intron Variant | AD |
rs2583435 | chr11:2937588 | T>C | SNV | Intergenic | AD |
rs2583442 | chr11:2934936 | T>C | SNV | Intergenic | AD |
rs1501576 | chr9:2918656 | T>C | SNV | Intergenic | AD |
rs17835089 | chr17:2907378 | G>C | SNV | RAP1GAP2 : Intron Variant | AD |
rs17022006 | chr3:2897050 | G>A | SNV | CNTN4 : Intron Variant | ND |
rs12677935 | chr8:2886993 | G>C | SNV | Intergenic | AD |
rs12676437 | chr8:2886750 | T>C | SNV | Intergenic | AD |
rs10488838 | chr4:2879608 | A>G | SNV | ADD1 : Intron Variant | AD |
rs7611373 | chr3:2875753 | G>A | SNV | CNTN4 : Intron Variant | AD |
rs2317457 | chr17:2849919 | G>A | SNV | RAP1GAP2 : Intron Variant | ND |
rs823243 | chr2:2844330 | T>C | SNV | Intergenic | AD |
rs231872 | chr11:2765831 | G>A / G>C / G>T | SNV | KCNQ1 : Intron Variant | ND |
rs231910 | chr11:2730055 | A>G | SNV | KCNQ1 : Intron Variant | ND |
rs2283214 | chr11:2729490 | G>A | SNV | KCNQ1 : Intron Variant | ND |
rs10903843 | chr10:2679970 | A>G | SNV | Intergenic | AD |
rs11597478 | chr10:2673226 | G>A | SNV | Intergenic | AD |
rs17158770 | chr10:2661380 | C>T | SNV | Intergenic | AD |
rs12574151 | chr11:2659888 | T>G | SNV | KCNQ1OT1 : Non Coding Transcript Variant KCNQ1 : Intron Variant | AD |
rs4741746 | chr9:2618969 | T>C | SNV | VLDLR-AS1 : Intron Variant | ND |
rs1479540 | chr3:2587793 | A>G | SNV | CNTN4 : Intron Variant | ND |
rs2728055 | chr3:2574606 | C>T | SNV | CNTN4 : Intron Variant | AD |
rs11707897 | chr3:2572942 | T>C | SNV | CNTN4 : Intron Variant | ND | AD |
rs6888228 | chr5:2553045 | T>C | SNV | Intergenic | AD |
rs7702425 | chr5:2549097 | A>G | SNV | Intergenic | AD |
rs2644171 | chr18:2540199 | A>G | SNV | METTL4 : Intron Variant | AD |
rs770224 | chr18:2533131 | T>C | SNV | Intergenic | AD |
rs11655295 | chr17:2530730 | G>T | SNV | Intergenic | ND |
rs7749514 | chr6:2524712 | C>T | SNV | Intergenic | AD |
rs462437 | chr5:2491471 | A>C / A>G / A>T | SNV | Intergenic | ND |
rs886277 | chr11:2418537 | T>C | SNV | TRPM5 : Missense Variant | AD |
rs6792956 | chr3:2371163 | T>C | SNV | CNTN4 : Intron Variant | ND |
rs12080256 | chr1:2319918 | C>A | SNV | Intergenic | AD |
rs2645077 | chr1:2317797 | G>A | SNV | Intergenic | AD |
rs2643902 | chr1:2314000 | T>C | SNV | Intergenic | AD |
rs4741657 | chr9:2239429 | T>C | SNV | LOC107987043 : Intron Variant | AD |
rs2376227 | chr9:2237390 | C>A | SNV | LOC107987043 : Intron Variant | AD |
rs2238043 | chr12:2166497 | G>A | SNV | CACNA1C : Intron Variant | ND |
rs17132242 | chr7:2139827 | G>A | SNV | MAD1L1 : Intron Variant | AD |
rs12776254 | chr10:2112668 | A>G | SNV | Intergenic | AD |
rs10413398 | chr19:2106697 | T>C | SNV | AP3D1 : Intron Variant | AD |
rs13269383 | chr8:2088699 | T>C | SNV | MYOM2 : Intron Variant | ND |
rs10512034 | chr9:2000684 | G>A | SNV | Intergenic | ND |
rs4141130 | chr12:1988550 | T>C | SNV | CACNA1C : Intron Variant DCP1B : Intron Variant | ND |
rs2252523 | chr16:1947613 | A>G | SNV | RPL3L : Intron Variant | AD |
rs6783551 | chr3:1943554 | T>C | SNV | Intergenic | AD |
rs4525524 | chr17:1941577 | T>C | SNV | RTN4RL1 : Intron Variant | AD |
rs4463305 | chr6:1918338 | T>C | SNV | GMDS : Intron Variant | AD |
rs4332037 | chr7:1911173 | C>T | SNV | MAD1L1 : Intron Variant | AD |
rs11041553 | chr11:1867725 | G>A | SNV | LSP1 : Intron Variant | AD |
rs2281760 | chr6:1866292 | A>C | SNV | GMDS : Intron Variant | AD |
rs749822 | chr8:1860090 | A>G | SNV | ARHGEF10 : Synonymous Variant | ND |
rs4807154 | chr19:1858874 | C>T | SNV | KLF16 : Intron Variant | AD |
rs17536666 | chr5:1844201 | T>C | SNV | Intergenic | ND |
rs4790825 | chr17:1842556 | A>G | SNV | RPA1 : Intron Variant | AD |
rs3800091 | chr6:1837594 | T>C | SNV | GMDS : Intron Variant | AD |
rs907609 | chr11:1836040 | C>T | SNV | SYT8 : Intron Variant | AD |
rs2887631 | chr12:1825415 | G>A | SNV | LRTM2 : Intron Variant CACNA2D4 : Intron Variant | AD |
rs12570407 | chr10:1812579 | C>T | SNV | Intergenic | AD |
rs6558545 | chr8:1808419 | G>A | SNV | Intergenic | AD |
rs3823270 | chr6:1781739 | A>G | SNV | GMDS : Intron Variant | ND |
rs10161408 | chr12:1779507 | T>C | SNV | ADIPOR2 : Intron Variant | AD |
rs3800043 | chr6:1764090 | C>T | SNV | GMDS : Intron Variant | AD |
rs1392466 | chr5:1744369 | G>A | SNV | Intergenic | AD |
rs17029209 | chr3:1739941 | T>C | SNV | Intergenic | AD |
rs1563188 | chr18:1738360 | A>G | SNV | Intergenic | AD |
rs6505955 | chr18:1731153 | A>G | SNV | Intergenic | AD |
rs7005715 | chr8:1701794 | G>A | SNV | DLGAP2 : 3 Prime UTR Variant | AD |
rs7825359 | chr8:1699869 | A>G | SNV | DLGAP2 : Intron Variant | AD |
rs17064176 | chr8:1652979 | G>A / G>T | SNV | DLGAP2 : Intron Variant | ND |
rs1535883 | chr20:1632173 | A>G | SNV | SIRPG : Intron Variant SIRPG-AS1 : 2KB Upstream Variant | ND |
rs3746722 | chr20:1630293 | G>A | SNV | SIRPG : Synonymous Variant | ND |
rs7086346 | chr10:1623626 | G>A / G>C | SNV | ADARB2 : Intron Variant | AD |
rs11250672 | chr10:1623271 | G>A | SNV | ADARB2 : Intron Variant | AD |
rs4790713 | chr17:1619583 | G>A | SNV | SLC43A2 : Intron Variant | AD |
rs702167 | chr9:1605827 | G>A | SNV | Intergenic | AD |
rs1112787 | chr10:1604704 | C>T | SNV | ADARB2 : Intron Variant | AD |
rs7252741 | chr19:1580335 | T>C | SNV | MBD3 : Intron Variant | AD |
rs2249431 | chr20:1552559 | T>C | SNV | SIRPD : Intron Variant | ND |
rs6705087 | chr2:1546537 | T>C | SNV | LOC102723730 : 2KB Upstream Variant | ND |
rs4927632 | chr2:1541338 | G>A | SNV | TPO : Intron Variant | ND |
rs4551123 | chr5:1536142 | A>G | SNV | Intergenic | AD |
rs6578492 | chr11:1534014 | A>G / A>T | SNV | Intergenic | AD |
rs2292453 | chr19:1526471 | G>A | SNV | PLK5 : Intron Variant | AD |
rs4608970 | chr5:1519082 | T>C | SNV | LPCAT1 : Intron Variant | AD |
rs17732233 | chr2:1515292 | C>T | SNV | TPO : Intron Variant | ND |
rs2963282 | chr5:1512093 | G>A | SNV | LPCAT1 : Intron Variant MIR6075 : 2KB Upstream Variant | AD |
rs6033557 | chr20:1367898 | A>G | SNV | FKBP1A-SDCBP2 : Intron Variant SDCBP2-AS1 : Intron Variant | ND |
rs17038032 | chr3:1347433 | C>T | SNV | CNTN6 : Intron Variant | AD |
rs9950729 | chr18:1344119 | T>C | SNV | LINC00470 : Intron Variant | AD |
rs10510170 | chr3:1333292 | A>G | SNV | CNTN6 : Intron Variant | AD |
rs7209096 | chr17:1325928 | G>A / G>C | SNV | Intergenic | ND |
rs2361573 | chr17:1322646 | T>C / T>G | SNV | Intergenic | ND |
rs17036851 | chr3:1263731 | G>A | SNV | CNTN6 : Intron Variant | ND |
rs6697886 | chr1:1238231 | G>A | SNV | Intergenic | AD |
rs7018922 | chr9:1230619 | T>C | SNV | Intergenic | AD |
rs11260542 | chr1:1174639 | A>G | SNV | TTLL10-AS1 : Non Coding Transcript Variant TTLL10 : Intron Variant | AD |
rs4971371 | chr2:1080998 | C>T | SNV | SNTG2 : Intron Variant | AD |
rs6474550 | chr9:1052722 | G>C / G>T | SNV | DMRT2 : Intron Variant | AD |
rs789046 | chr18:1020819 | A>G / A>T | SNV | LOC107985165 : Intron Variant | AD |
rs16954588 | chr18:1014559 | C>T | SNV | LOC107985165 : Intron Variant | AD |
rs789071 | chr18:1008338 | G>A | SNV | LOC107985165 : Intron Variant | AD |
rs4807395 | chr19:1002848 | A>G | SNV | GRIN3B : Intron Variant | AD |
rs7249037 | chr19:988136 | G>A | SNV | WDR18 : Intron Variant | AD |
rs3817576 | chr7:983555 | A>G | SNV | C7orf50 : Intron Variant CYP2W1 : Intron Variant | AD |
rs10272099 | chr7:977312 | T>C | SNV | COX19 : 2KB Upstream Variant | AD |
rs16868701 | chr5:964135 | G>A | SNV | Intergenic | AD |
rs1637995 | chr19:960445 | A>G | SNV | ARID3A : Intron Variant | AD |
rs6413436 | chr12:913513 | A>G | SNV | RAD52 : Intron Variant | AD |
rs4816051 | chr20:893106 | T>C / T>G | SNV | ANGPT4 : Intron Variant | ND |
rs11246327 | chr11:840034 | C>A | SNV | POLR2L : 3 Prime UTR Variant | AD |
rs7963376 | chr12:817082 | T>C | SNV | WNK1 : Intron Variant | AD |
rs10774464 | chr12:813242 | C>T | SNV | WNK1 : Intron Variant | AD |
rs10902222 | chr11:810882 | G>T | SNV | RPLP2 : Intron Variant PIDD1 : 2KB Upstream Variant SNORA52 : 2KB Upstream Variant | AD |
rs7035993 | chr9:786996 | A>G | SNV | Intergenic | ND |
rs7930569 | chr11:771034 | A>G | SNV | PDDC1 : Synonymous Variant | AD |
rs6054627 | chr20:767191 | A>G | SNV | SLC52A3 : Intron Variant | AD |
rs10758863 | chr9:742642 | T>G | SNV | KANK1 : Intron Variant | ND |
rs13286166 | chr9:741307 | G>A | SNV | KANK1 : Intron Variant | ND |
rs7027152 | chr9:741001 | T>C | SNV | KANK1 : Intron Variant | ND |
rs10739127 | chr9:737436 | G>T | SNV | KANK1 : Intron Variant | ND |
rs10815562 | chr9:732302 | T>C | SNV | KANK1 : Intron Variant | ND |
rs6117232 | chr20:708893 | C>T | SNV | Intergenic | AD |
rs4742236 | chr9:686753 | G>A | SNV | KANK1 : Intron Variant | ND |
rs4742225 | chr9:677938 | G>T | SNV | KANK1 : Intron Variant | ND |
rs502396 | chr18:659236 | C>T | SNV | TYMS : Intron Variant TYMSOS : 2KB Upstream Variant | AD |
rs6489683 | chr12:627548 | G>A | SNV | NINJ2 : Intron Variant | ND |
rs7033109 | chr9:614905 | C>T | SNV | KANK1 : Intron Variant | AD |
rs7020705 | chr9:614803 | G>C | SNV | KANK1 : Intron Variant | AD |
rs4610808 | chr9:614707 | C>G | SNV | KANK1 : Intron Variant | AD |
rs7047247 | chr9:613932 | G>A | SNV | KANK1 : Intron Variant | AD |
rs1962203 | chr9:613215 | A>G | SNV | KANK1 : Intron Variant | AD |
rs10975395 | chr9:609829 | T>C | SNV | KANK1 : Intron Variant | AD |
rs2804308 | chr9:607382 | C>G | SNV | KANK1 : Intron Variant | AD |
rs2804304 | chr9:606439 | T>C | SNV | KANK1 : Intron Variant | AD |
rs2641996 | chr9:595756 | A>C / A>T | SNV | KANK1 : Intron Variant | AD |
rs2641997 | chr9:594697 | G>T | SNV | KANK1 : Intron Variant | AD |
rs2642001 | chr9:593229 | T>C | SNV | KANK1 : Intron Variant | AD |
rs2642002 | chr9:592718 | C>T | SNV | KANK1 : Intron Variant | AD |
rs2642003 | chr9:592229 | T>C | SNV | KANK1 : Intron Variant | AD |
rs2804280 | chr9:589511 | C>T | SNV | KANK1 : Intron Variant | AD |
rs2641970 | chr9:581453 | C>T | SNV | KANK1 : Intron Variant | AD |
rs11136864 | chr8:581083 | A>C | SNV | Intergenic | AD |
rs2361089 | chr9:580868 | C>T | SNV | KANK1 : Intron Variant | AD |
rs2804276 | chr9:580725 | T>C | SNV | KANK1 : Intron Variant | AD |
rs2804275 | chr9:580319 | G>A | SNV | KANK1 : Intron Variant | AD |
rs2641973 | chr9:580171 | A>T | SNV | KANK1 : Intron Variant | AD |
rs2804266 | chr9:568384 | T>C | SNV | KANK1 : Intron Variant | AD |
rs4740817 | chr9:561143 | C>T | SNV | KANK1 : Intron Variant | ND |
rs10975061 | chr9:543631 | C>T | SNV | KANK1 : Intron Variant | ND |
rs2075033 | chr12:535171 | G>A | SNV | B4GALNT3 : Missense Variant | AD |
rs7678962 | chr4:523409 | G>A | SNV | PIGG : Intron Variant | AD |
rs2026075 | chr9:520886 | G>A | SNV | KANK1 : Intron Variant | ND |
rs1928415 | chr9:517715 | C>T | SNV | KANK1 : Intron Variant | ND |
rs7038366 | chr9:515616 | C>A | SNV | KANK1 : Intron Variant | ND |
rs12372234 | chr12:449257 | C>T | SNV | Intergenic | AD |
rs61908460 | chr12:414895 | C>T | SNV | CCDC77 : Intron Variant | AD |
rs12346176 | chr9:398673 | A>C / A>G | SNV | DOCK8 : Intron Variant | AD |
rs12348944 | chr9:377066 | C>T | SNV | DOCK8 : Synonymous Variant | ND |
rs9319629 | chr17:373191 | G>A | SNV | RPH3AL : Intron Variant | AD |
rs6740249 | chr2:355800 | T>C | SNV | Intergenic | AD |
rs9654453 | chr5:299506 | T>C | SNV | PDCD6 : Intron Variant | AD |
rs525381 | chr12:275626 | G>A | SNV | Intergenic | AD |
rs12450789 | chr17:220063 | C>T | SNV | RPH3AL : Intron Variant | AD |
rs11150884 | chr17:212735 | T>C | SNV | RPH3AL : Non Coding Transcript Variant | ND |
rs6899567 | chr6:212595 | G>A | SNV | Intergenic | AD |
rs11654695 | chr17:209189 | C>T | SNV | Intergenic | ND |
rs12146505 | chr11:1068233 | T>G | SNV | LOC107987157 : Intron Variant | AD |
rs12672125 | chr7:116054 | T>C | SNV | LOC105375114 : Intron Variant | CD |
rs9856879 | chr3:107042 | T>C | SNV | Intergenic | AD |
rs6443038 | chr3:91729 | G>A | SNV | Intergenic | AD |
rs11674512 | chr2:239773817 | A>G | SNV | LOC150935 : Intron Variant | AD |
rs6748389 | chr2:239763879 | T>G | SNV | LOC150935 : Intron Variant | AD |
rs17042708 | chr3:66543 | A>G | SNV | LOC105376921 : Intron Variant LOC107986040 : 2KB Upstream Variant | AD |
rs991639 | chr3:47829 | A>C | SNV | Intergenic | AD |