rs6473310

Homo sapiens
A>G / A>T
None
Check p-value
SNV (Single Nucleotide Variation)
A==0341 (10206/29924,GnomAD)
A==0356 (10384/29118,TOPMED)
A==0393 (1968/5008,1000G)
A==0332 (1281/3854,ALSPAC)
A==0320 (1188/3708,TWINSUK)
chr8:81795746 (GRCh38.p7) (8q21.13)
AD
GWASdb2
1   publication(s)
See rs on genome
20 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 8NC_000008.11:g.81795746A>G
GRCh38.p7 chr 8NC_000008.11:g.81795746A>T
GRCh37.p13 chr 8NC_000008.10:g.82707981A>G
GRCh37.p13 chr 8NC_000008.10:g.82707981A>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.362G=0.638
1000GenomesAmericanSub694A=0.390G=0.610
1000GenomesEast AsianSub1008A=0.597G=0.403
1000GenomesEuropeSub1006A=0.327G=0.673
1000GenomesGlobalStudy-wide5008A=0.393G=0.607
1000GenomesSouth AsianSub978A=0.290G=0.710
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.332G=0.668
The Genome Aggregation DatabaseAfricanSub8710A=0.361G=0.639
The Genome Aggregation DatabaseAmericanSub838A=0.320G=0.68,
The Genome Aggregation DatabaseEast AsianSub1610A=0.629G=0.371
The Genome Aggregation DatabaseEuropeSub18464A=0.307G=0.692
The Genome Aggregation DatabaseGlobalStudy-wide29924A=0.341G=0.658
The Genome Aggregation DatabaseOtherSub302A=0.370G=0.63,
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.356G=0.643
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.320G=0.680
PMID Title Author Journal
23743675A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.Kapoor MHum Genet

P-Value

SNP ID p-value Traits Study
rs64733103.42E-05alcohol consumption23743675

eQTL of rs6473310 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 rs6473310 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 )
chr8101773554101775046E068-33919
chr8101847470101848214E06838505
chr8101762717101763214E071-45751
chr8101764400101764498E071-44467
chr8101764560101764751E071-44214
chr8101764770101764823E071-44142
chr8101803597101803661E072-5304
chr8101803758101804338E074-4627
chr8101804391101804510E074-4455
chr8101847470101848214E07438505
chr8101848259101848339E07439294
chr8101775773101775823E081-33142
chr8101775832101775882E081-33083
chr8101775951101776079E081-32886
chr8101803597101803661E081-5304
chr8101803758101804338E081-4627
chr8101804391101804510E081-4455
chr8101851627101851825E08142662
chr8101851845101851917E08142880
chr8101775334101775644E082-33321