rs7955309

Homo sapiens
T>C
RERG : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
C=0362 (10851/29916,GnomAD)
C=0373 (10888/29118,TOPMED)
C=0343 (1716/5008,1000G)
C=0317 (1222/3854,ALSPAC)
C=0331 (1227/3708,TWINSUK)
chr12:15215264 (GRCh38.p7) (12p12.3)
AD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 12NC_000012.12:g.15215264T>C
GRCh37.p13 chr 12NC_000012.11:g.15368198T>C

Gene: RERG, RAS like estrogen regulated growth inhibitor(minus strand)

Molecule type Change Amino acid[Codon] SO Term
RERG transcript variant 2NM_001190726.1:c.N/AIntron Variant
RERG transcript variant 1NM_032918.2:c.N/AIntron Variant
RERG transcript variant X1XM_017020121.1:c.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.481C=0.519
1000GenomesAmericanSub694T=0.790C=0.210
1000GenomesEast AsianSub1008T=0.755C=0.245
1000GenomesEuropeSub1006T=0.651C=0.349
1000GenomesGlobalStudy-wide5008T=0.657C=0.343
1000GenomesSouth AsianSub978T=0.710C=0.290
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.683C=0.317
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.626C=0.373
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.669C=0.331
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs79553090.000473alcohol dependence20201924

eQTL of rs7955309 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs7955309 in Fetal Brain

Probe ID Position Gene beta p-value
There is no meQTL annotation for this SNP

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr121537509615375150E0676898
chr121537526515375417E0677067
chr121531944415319504E068-48694
chr121532026115320338E068-47860
chr121532039615320436E068-47762
chr121533235815332815E068-35383
chr121533281615332929E068-35269
chr121533294915333203E068-34995
chr121533332215333493E068-34705
chr121533353715333639E068-34559
chr121533367015333829E068-34369
chr121533406015334535E068-33663
chr121533457115334669E068-33529
chr121533470115334936E068-33262
chr121533958715339889E068-28309
chr121533994915340050E068-28148
chr121534689115347350E068-20848
chr121534737215347448E068-20750
chr121534749515347641E068-20557
chr121534807015348846E068-19352
chr121536056815360622E068-7576
chr121536069215360742E068-7456
chr121536876315368813E068565
chr121536893115369131E068733
chr121537509615375150E0686898
chr121537526515375417E0687067
chr121539315415393198E07024956
chr121533281615332929E071-35269
chr121533294915333203E071-34995
chr121533332215333493E071-34705
chr121537509615375150E0726898
chr121537526515375417E0727067
chr121534628215346469E081-21729
chr121534807015348846E081-19352
chr121536428215364381E081-3817
chr121536553415365599E081-2599
chr121536560515365883E081-2315
chr121536664615367166E081-1032
chr121537509615375150E0816898
chr121534661515346858E082-21340
chr121534689115347350E082-20848
chr121534737215347448E082-20750
chr121534749515347641E082-20557
chr121536553415365599E082-2599
chr121536560515365883E082-2315







Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr121537345815374927E0675260
chr121537221715372267E0684019
chr121537227415372324E0684076
chr121537236715372417E0684169
chr121537243915372489E0684241
chr121537269415372746E0684496
chr121537278115372838E0684583
chr121537287115373126E0684673
chr121537313815373387E0684940
chr121537345815374927E0685260
chr121537345815374927E0695260
chr121537345815374927E0705260
chr121537345815374927E0715260
chr121537345815374927E0725260
chr121537287115373126E0734673
chr121537313815373387E0734940
chr121537345815374927E0735260
chr121537345815374927E0745260