rs9291662

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0342 (10254/29952,GnomAD)
A=0415 (12102/29118,TOPMED)
A=0416 (2083/5008,1000G)
A=0214 (823/3854,ALSPAC)
A=0223 (827/3708,TWINSUK)
chr4:18077894 (GRCh38.p7) (4p15.31)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 4NC_000004.12:g.18077894G>A
GRCh37.p13 chr 4NC_000004.11:g.18079517G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.321A=0.679
1000GenomesAmericanSub694G=0.630A=0.370
1000GenomesEast AsianSub1008G=0.498A=0.502
1000GenomesEuropeSub1006G=0.780A=0.220
1000GenomesGlobalStudy-wide5008G=0.584A=0.416
1000GenomesSouth AsianSub978G=0.790A=0.210
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.786A=0.214
The Genome Aggregation DatabaseAfricanSub8714G=0.379A=0.621
The Genome Aggregation DatabaseAmericanSub838G=0.650A=0.350
The Genome Aggregation DatabaseEast AsianSub1620G=0.475A=0.525
The Genome Aggregation DatabaseEuropeSub18478G=0.803A=0.196
The Genome Aggregation DatabaseGlobalStudy-wide29952G=0.657A=0.342
The Genome Aggregation DatabaseOtherSub302G=0.790A=0.210
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.584A=0.415
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.777A=0.223
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
rs92916620.0001alcoholism (heaviness of drinking)21529783

eQTL of rs9291662 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 rs9291662 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.