rs6808582

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0199 (5938/29842,GnomAD)
A=0270 (7889/29118,TOPMED)
A=0208 (1041/5008,1000G)
A=0104 (400/3854,ALSPAC)
A=0108 (399/3708,TWINSUK)
chr3:164869771 (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.164869771G>A
GRCh37.p13 chr 3NC_000003.11:g.164587559G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.506A=0.494
1000GenomesAmericanSub694G=0.900A=0.100
1000GenomesEast AsianSub1008G=0.902A=0.098
1000GenomesEuropeSub1006G=0.906A=0.094
1000GenomesGlobalStudy-wide5008G=0.792A=0.208
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 DatabaseAfricanSub8678G=0.535A=0.465
The Genome Aggregation DatabaseAmericanSub838G=0.920A=0.080
The Genome Aggregation DatabaseEast AsianSub1610G=0.892A=0.108
The Genome Aggregation DatabaseEuropeSub18414G=0.911A=0.088
The Genome Aggregation DatabaseGlobalStudy-wide29842G=0.801A=0.199
The Genome Aggregation DatabaseOtherSub302G=0.910A=0.090
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.729A=0.270
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
rs68085824.99E-09alcohol dependence (age at onset)24962325

eQTL of rs6808582 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 rs6808582 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.