rs2968625

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G=0323 (9682/29892,GnomAD)
G=0308 (8985/29116,TOPMED)
G=0279 (1398/5008,1000G)
G=0381 (1469/3854,ALSPAC)
G=0362 (1341/3708,TWINSUK)
chr2:35938765 (GRCh38.p7) (2p22.3)
AD
GWASdb2
1   publication(s)
See rs on genome
8 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.35938765G>A
GRCh37.p13 chr 2NC_000002.11:g.36163832A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.787G==0.213
1000GenomesAmericanSub694A=0.740G==0.260
1000GenomesEast AsianSub1008A=0.747G==0.253
1000GenomesEuropeSub1006A=0.590G==0.410
1000GenomesGlobalStudy-wide5008A=0.721G==0.279
1000GenomesSouth AsianSub978A=0.720G==0.280
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.619G==0.381
The Genome Aggregation DatabaseAfricanSub8710A=0.769G==0.231
The Genome Aggregation DatabaseAmericanSub834A=0.780G==0.220
The Genome Aggregation DatabaseEast AsianSub1620A=0.771G==0.229
The Genome Aggregation DatabaseEuropeSub18428A=0.620G==0.379
The Genome Aggregation DatabaseGlobalStudy-wide29892A=0.676G==0.323
The Genome Aggregation DatabaseOtherSub300A=0.610G==0.390
Trans-Omics for Precision MedicineGlobalStudy-wide29116A=0.691G==0.308
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.638G==0.362
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
rs29686250.000403alcohol dependence20201924

eQTL of rs2968625 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 rs2968625 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 )
chr23619882036198887E06834988
chr23619893736199129E06835105
chr23617507736175121E07011245
chr23617530636175413E07011474
chr23617272236173230E0748890
chr23618836336188427E08224531
chr23618843736188537E08224605
chr23618857736188705E08224745