rs4832336

Homo sapiens
G>A / G>C
None
Check p-value
SNV (Single Nucleotide Variation)
A=0291 (8705/29874,GnomAD)
A=0307 (8960/29116,TOPMED)
A=0318 (1591/5008,1000G)
A=0230 (887/3854,ALSPAC)
A=0236 (875/3708,TWINSUK)
chr2:83830839 (GRCh38.p7) (2p11.2)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.83830839G>A
GRCh38.p7 chr 2NC_000002.12:g.83830839G>C
GRCh37.p13 chr 2NC_000002.11:g.84057963G>A
GRCh37.p13 chr 2NC_000002.11:g.84057963G>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.675A=0.325
1000GenomesAmericanSub694G=0.660A=0.340
1000GenomesEast AsianSub1008G=0.500A=0.500
1000GenomesEuropeSub1006G=0.744A=0.256
1000GenomesGlobalStudy-wide5008G=0.682A=0.318
1000GenomesSouth AsianSub978G=0.830A=0.170
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.770A=0.230
The Genome Aggregation DatabaseAfricanSub8666G=0.682A=0.318
The Genome Aggregation DatabaseAmericanSub838G=0.600A=0.400
The Genome Aggregation DatabaseEast AsianSub1610G=0.499A=0.501
The Genome Aggregation DatabaseEuropeSub18458G=0.743A=0.256
The Genome Aggregation DatabaseGlobalStudy-wide29874G=0.708A=0.291
The Genome Aggregation DatabaseOtherSub302G=0.780A=0.220
Trans-Omics for Precision MedicineGlobalStudy-wide29116G=0.692A=0.307
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.764A=0.236
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
rs48323360.00051alcohol dependence20201924

eQTL of rs4832336 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 rs4832336 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.