rs2582662

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0431 (12917/29934,GnomAD)
G==0467 (13608/29118,TOPMED)
A=0447 (2239/5008,1000G)
G==0383 (1476/3854,ALSPAC)
G==0359 (1330/3708,TWINSUK)
chr5:16272528 (GRCh38.p7) (5p15.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.16272528G>A
GRCh37.p13 chr 5NC_000005.9:g.16272637G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.601A=0.399
1000GenomesAmericanSub694G=0.560A=0.440
1000GenomesEast AsianSub1008G=0.812A=0.188
1000GenomesEuropeSub1006G=0.356A=0.644
1000GenomesGlobalStudy-wide5008G=0.553A=0.447
1000GenomesSouth AsianSub978G=0.420A=0.580
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.383A=0.617
The Genome Aggregation DatabaseAfricanSub8716G=0.568A=0.432
The Genome Aggregation DatabaseAmericanSub836G=0.580A=0.420
The Genome Aggregation DatabaseEast AsianSub1614G=0.813A=0.187
The Genome Aggregation DatabaseEuropeSub18468G=0.327A=0.672
The Genome Aggregation DatabaseGlobalStudy-wide29934G=0.431A=0.568
The Genome Aggregation DatabaseOtherSub300G=0.390A=0.610
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.467A=0.532
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.359A=0.641
PMID Title Author Journal
21529783A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.Heath ACBiol Psychiatry

P-Value

SNP ID p-value Traits Study
rs25826622.6E-05alcoholism (heaviness of drinking)21529783

eQTL of rs2582662 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 rs2582662 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.