Sequence Name | Change(s) |
---|---|
GRCh38.p7 chr 9 | NC_000009.12:g.7067344G>C |
GRCh37.p13 chr 9 | NC_000009.11:g.7067344G>C |
Molecule type | Change | Amino acid[Codon] | SO Term |
---|---|---|---|
KDM4C transcript variant 3 | NM_001146695.1:c. | N/A | Intron Variant |
KDM4C transcript variant 4 | NM_001146696.1:c. | N/A | Intron Variant |
KDM4C transcript variant 5 | NM_001304339.1:c. | N/A | Intron Variant |
KDM4C transcript variant 6 | NM_001304340.1:c. | N/A | Intron Variant |
KDM4C transcript variant 1 | NM_015061.3:c. | N/A | Intron Variant |
KDM4C transcript variant 7 | NM_001304341.1:c. | N/A | Genic Downstream Transcript Variant |
KDM4C transcript variant 8 | NR_130707.1:n. | N/A | Genic Downstream Transcript Variant |
KDM4C transcript variant X1 | XM_006716741.2:c. | N/A | Intron Variant |
KDM4C transcript variant X4 | XM_011517811.2:c. | N/A | Intron Variant |
KDM4C transcript variant X6 | XM_011517812.2:c. | N/A | Intron Variant |
KDM4C transcript variant X14 | XM_011517816.2:c. | N/A | Intron Variant |
KDM4C transcript variant X2 | XM_017014498.1:c. | N/A | Intron Variant |
KDM4C transcript variant X3 | XM_017014499.1:c. | N/A | Intron Variant |
KDM4C transcript variant X5 | XM_017014500.1:c. | N/A | Intron Variant |
KDM4C transcript variant X7 | XM_017014501.1:c. | N/A | Intron Variant |
KDM4C transcript variant X13 | XM_017014503.1:c. | N/A | Intron Variant |
KDM4C transcript variant X16 | XM_017014505.1:c. | N/A | Intron Variant |
KDM4C transcript variant X17 | XM_017014506.1:c. | N/A | Intron Variant |
KDM4C transcript variant X9 | XM_017014502.1:c. | N/A | Genic Downstream Transcript Variant |
KDM4C transcript variant X15 | XM_017014504.1:c. | N/A | Genic Downstream Transcript Variant |
KDM4C transcript variant X8 | XR_001746252.1:n. | N/A | Intron Variant |
KDM4C transcript variant X10 | XR_001746253.1:n. | N/A | Intron Variant |
KDM4C transcript variant X11 | XR_001746254.1:n. | N/A | Intron Variant |
KDM4C transcript variant X12 | XR_001746255.1:n. | N/A | Intron Variant |
Study | Population | Group | Sample # | Ref Allele | Alt Allele |
---|---|---|---|---|---|
1000Genomes | African | Sub | 1322 | G=0.722 | C=0.278 |
1000Genomes | American | Sub | 694 | G=0.680 | C=0.320 |
1000Genomes | East Asian | Sub | 1008 | G=0.810 | C=0.190 |
1000Genomes | Europe | Sub | 1006 | G=0.544 | C=0.456 |
1000Genomes | Global | Study-wide | 5008 | G=0.714 | C=0.286 |
1000Genomes | South Asian | Sub | 978 | G=0.800 | C=0.200 |
The Avon Longitudinal Study of Parents and Children | PARENT AND CHILD COHORT | Study-wide | 3854 | G=0.540 | C=0.460 |
The Genome Aggregation Database | African | Sub | 8708 | G=0.703 | C=0.297 |
The Genome Aggregation Database | American | Sub | 838 | G=0.710 | C=0.290 |
The Genome Aggregation Database | East Asian | Sub | 1622 | G=0.819 | C=0.181 |
The Genome Aggregation Database | Europe | Sub | 18462 | G=0.509 | C=0.491 |
The Genome Aggregation Database | Global | Study-wide | 29932 | G=0.589 | C=0.410 |
The Genome Aggregation Database | Other | Sub | 302 | G=0.660 | C=0.340 |
Trans-Omics for Precision Medicine | Global | Study-wide | 29118 | G=0.641 | C=0.358 |
UK 10K study - Twins | TWIN COHORT | Study-wide | 3708 | G=0.551 | C=0.449 |
PMID | Title | Author | Journal |
---|---|---|---|
19268276 | Genome-wide association study of smoking initiation and current smoking. | Vink JM | Am J Hum Genet |
SNP ID | p-value | Traits | Study |
---|---|---|---|
rs7034275 | 0.000381 | nicotine smoking | 19268276 |
Position (v37) | eGene | GeneID | Variant | p-value | TSS | Tissue | |
---|---|---|---|---|---|---|---|
There is no eQTL annotation for this SNP |
Probe ID | Position | Gene | beta | p-value | |||
---|---|---|---|---|---|---|---|
There is no meQTL annotation for this SNP |
There is no significant Hi-C chromatin interaction data for this SNP.
Chromosome | Start | End | Region | Distance ( -/+ : Up/Downstream ) |
---|---|---|---|---|
chr9 | 7052503 | 7053138 | E068 | -14206 |
chr9 | 7056766 | 7057012 | E068 | -10332 |
chr9 | 7057223 | 7057335 | E068 | -10009 |
chr9 | 7057342 | 7057422 | E068 | -9922 |
chr9 | 7057457 | 7058000 | E068 | -9344 |
chr9 | 7058090 | 7058230 | E068 | -9114 |
chr9 | 7058310 | 7058379 | E068 | -8965 |
chr9 | 7058388 | 7058453 | E068 | -8891 |
chr9 | 7058500 | 7058568 | E068 | -8776 |
chr9 | 7085202 | 7085252 | E068 | 17858 |
chr9 | 7085361 | 7085412 | E068 | 18017 |
chr9 | 7052503 | 7053138 | E069 | -14206 |
chr9 | 7053246 | 7053364 | E069 | -13980 |
chr9 | 7053377 | 7053446 | E069 | -13898 |
chr9 | 7053484 | 7053547 | E069 | -13797 |
chr9 | 7057457 | 7058000 | E069 | -9344 |
chr9 | 7058090 | 7058230 | E069 | -9114 |
chr9 | 7078796 | 7079177 | E069 | 11452 |
chr9 | 7082561 | 7082720 | E069 | 15217 |
chr9 | 7085202 | 7085252 | E069 | 17858 |
chr9 | 7085361 | 7085412 | E069 | 18017 |
chr9 | 7088153 | 7088231 | E069 | 20809 |
chr9 | 7088301 | 7088405 | E069 | 20957 |
chr9 | 7037273 | 7037323 | E070 | -30021 |
chr9 | 7084789 | 7084843 | E071 | 17445 |
chr9 | 7085202 | 7085252 | E071 | 17858 |
chr9 | 7085361 | 7085412 | E071 | 18017 |
chr9 | 7082561 | 7082720 | E072 | 15217 |
chr9 | 7052503 | 7053138 | E073 | -14206 |
chr9 | 7053246 | 7053364 | E073 | -13980 |
chr9 | 7053377 | 7053446 | E073 | -13898 |
chr9 | 7056387 | 7056589 | E074 | -10755 |
chr9 | 7056766 | 7057012 | E074 | -10332 |
chr9 | 7057457 | 7058000 | E074 | -9344 |
chr9 | 7078796 | 7079177 | E074 | 11452 |
chr9 | 7084789 | 7084843 | E074 | 17445 |
chr9 | 7085202 | 7085252 | E074 | 17858 |
chr9 | 7085361 | 7085412 | E074 | 18017 |
chr9 | 7115746 | 7115884 | E074 | 48402 |
chr9 | 7052503 | 7053138 | E081 | -14206 |
chr9 | 7053246 | 7053364 | E081 | -13980 |
chr9 | 7053377 | 7053446 | E081 | -13898 |
chr9 | 7053246 | 7053364 | E082 | -13980 |
chr9 | 7053377 | 7053446 | E082 | -13898 |
chr9 | 7055053 | 7055161 | E082 | -12183 |
chr9 | 7088501 | 7089004 | E082 | 21157 |
chr9 | 7089202 | 7089715 | E082 | 21858 |