rs1500422

Homo sapiens
G>A / G>C
None
Check p-value
SNV (Single Nucleotide Variation)
A=0268 (8001/29814,GnomAD)
A=0219 (6380/29118,TOPMED)
A=0167 (838/5008,1000G)
A=0364 (1401/3854,ALSPAC)
A=0366 (1357/3708,TWINSUK)
chr3:20678646 (GRCh38.p7) (3p24.3)
AD
GWASdb2
1   publication(s)
See rs on genome
1 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.20678646G>A
GRCh38.p7 chr 3NC_000003.12:g.20678646G>C
GRCh37.p13 chr 3NC_000003.11:g.20720138G>A
GRCh37.p13 chr 3NC_000003.11:g.20720138G>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.956A=0.044
1000GenomesAmericanSub694G=0.700A=0.300
1000GenomesEast AsianSub1008G=0.970A=0.030
1000GenomesEuropeSub1006G=0.652A=0.348
1000GenomesGlobalStudy-wide5008G=0.833A=0.167
1000GenomesSouth AsianSub978G=0.810A=0.190
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.636A=0.364
The Genome Aggregation DatabaseAfricanSub8700G=0.918A=0.082
The Genome Aggregation DatabaseAmericanSub818G=0.650A=0.350
The Genome Aggregation DatabaseEast AsianSub1620G=0.978A=0.022
The Genome Aggregation DatabaseEuropeSub18374G=0.626A=0.373
The Genome Aggregation DatabaseGlobalStudy-wide29814G=0.731A=0.268
The Genome Aggregation DatabaseOtherSub302G=0.630A=0.370
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.780A=0.219
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.634A=0.366
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
rs15004220.000631alcohol dependence20201924

eQTL of rs1500422 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 rs1500422 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 )
chr366063146606427E081-30761