rs7468695

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0119 (3585/29936,GnomAD)
G==0110 (3212/29102,TOPMED)
G==0140 (701/5008,1000G)
G==0086 (333/3854,ALSPAC)
G==0084 (311/3708,TWINSUK)
chr9:27234523 (GRCh38.p7) (9p21.2)
AD
GWASdb2
1   publication(s)
See rs on genome
6 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.27234523G>A
GRCh37.p13 chr 9NC_000009.11:g.27234521G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.151A=0.849
1000GenomesAmericanSub694G=0.110A=0.890
1000GenomesEast AsianSub1008G=0.220A=0.780
1000GenomesEuropeSub1006G=0.089A=0.911
1000GenomesGlobalStudy-wide5008G=0.140A=0.860
1000GenomesSouth AsianSub978G=0.120A=0.880
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.086A=0.914
The Genome Aggregation DatabaseAfricanSub8716G=0.145A=0.855
The Genome Aggregation DatabaseAmericanSub834G=0.160A=0.840
The Genome Aggregation DatabaseEast AsianSub1614G=0.224A=0.776
The Genome Aggregation DatabaseEuropeSub18470G=0.097A=0.902
The Genome Aggregation DatabaseGlobalStudy-wide29936G=0.119A=0.880
The Genome Aggregation DatabaseOtherSub302G=0.070A=0.930
Trans-Omics for Precision MedicineGlobalStudy-wide29102G=0.110A=0.889
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.084A=0.916
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
rs74686950.00046Alcohol dependence (early age of onset)20201924
rs74686950.00094alcohol dependence20201924

eQTL of rs7468695 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 rs7468695 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 )
chr92727592227276869E07041401
chr92728025627280363E07045735
chr92728037827280428E07045857
chr92728025627280363E08145735
chr92728037827280428E08145857
chr92727592227276869E08241401