rs56303997

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0180 (5394/29898,GnomAD)
A=0240 (6997/29118,TOPMED)
A=0192 (961/5008,1000G)
A=0104 (401/3854,ALSPAC)
A=0108 (400/3708,TWINSUK)
chr3:164871362 (GRCh38.p7) (3q26.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.164871362G>A
GRCh37.p13 chr 3NC_000003.11:g.164589150G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.562A=0.438
1000GenomesAmericanSub694G=0.910A=0.090
1000GenomesEast AsianSub1008G=0.906A=0.094
1000GenomesEuropeSub1006G=0.904A=0.096
1000GenomesGlobalStudy-wide5008G=0.808A=0.192
1000GenomesSouth AsianSub978G=0.870A=0.130
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.896A=0.104
The Genome Aggregation DatabaseAfricanSub8690G=0.597A=0.403
The Genome Aggregation DatabaseAmericanSub836G=0.930A=0.070
The Genome Aggregation DatabaseEast AsianSub1612G=0.900A=0.100
The Genome Aggregation DatabaseEuropeSub18458G=0.910A=0.089
The Genome Aggregation DatabaseGlobalStudy-wide29898G=0.819A=0.180
The Genome Aggregation DatabaseOtherSub302G=0.900A=0.100
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.759A=0.240
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.892A=0.108
PMID Title Author Journal
24962325Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families.Kapoor MDrug Alcohol Depend

P-Value

SNP ID p-value Traits Study
rs563039979.02E-09alcohol dependence (age at onset)24962325

eQTL of rs56303997 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 rs56303997 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.