rs11914608

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0367 (11000/29908,GnomAD)
G=0324 (9457/29118,TOPMED)
G=0267 (1336/5008,1000G)
G=0462 (1781/3854,ALSPAC)
G=0483 (1790/3708,TWINSUK)
chr3:18662807 (GRCh38.p7) (3p24.3)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.18662807A>G
GRCh37.p13 chr 3NC_000003.11:g.18704299A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.845G=0.155
1000GenomesAmericanSub694A=0.720G=0.280
1000GenomesEast AsianSub1008A=0.827G=0.173
1000GenomesEuropeSub1006A=0.564G=0.436
1000GenomesGlobalStudy-wide5008A=0.733G=0.267
1000GenomesSouth AsianSub978A=0.670G=0.330
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.538G=0.462
The Genome Aggregation DatabaseAfricanSub8708A=0.810G=0.190
The Genome Aggregation DatabaseAmericanSub836A=0.670G=0.330
The Genome Aggregation DatabaseEast AsianSub1602A=0.836G=0.164
The Genome Aggregation DatabaseEuropeSub18460A=0.528G=0.471
The Genome Aggregation DatabaseGlobalStudy-wide29908A=0.632G=0.367
The Genome Aggregation DatabaseOtherSub302A=0.660G=0.340
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.675G=0.324
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.517G=0.483
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
rs119146080.000014Alcohol dependence (early age of onset)20201924
rs119146080.0000142alcoholismpha002892
rs119146080.00023alcohol dependence20201924

eQTL of rs11914608 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 rs11914608 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.