rs11936591

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0056 (1673/29880,GnomAD)
T=0051 (1489/29118,TOPMED)
T=0073 (364/5008,1000G)
T=0032 (122/3854,ALSPAC)
T=0023 (84/3708,TWINSUK)
chr4:133233577 (GRCh38.p7) (4q28.3)
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.133233577C>T
GRCh37.p13 chr 4NC_000004.11:g.134154732C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.902T=0.098
1000GenomesAmericanSub694C=0.950T=0.050
1000GenomesEast AsianSub1008C=0.904T=0.096
1000GenomesEuropeSub1006C=0.968T=0.032
1000GenomesGlobalStudy-wide5008C=0.927T=0.073
1000GenomesSouth AsianSub978C=0.930T=0.070
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.968T=0.032
The Genome Aggregation DatabaseAfricanSub8706C=0.925T=0.075
The Genome Aggregation DatabaseAmericanSub838C=0.950T=0.050
The Genome Aggregation DatabaseEast AsianSub1622C=0.921T=0.079
The Genome Aggregation DatabaseEuropeSub18412C=0.953T=0.046
The Genome Aggregation DatabaseGlobalStudy-wide29880C=0.944T=0.056
The Genome Aggregation DatabaseOtherSub302C=0.990T=0.010
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.948T=0.051
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.977T=0.023
PMID Title Author Journal
23953852Genome-wide association studies of maximum number of drinks.Pan YJ Psychiatr Res

P-Value

SNP ID p-value Traits Study
rs119365919.95E-05alcohol consumption23953852

eQTL of rs11936591 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 rs11936591 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.