rs4891112

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0312 (9374/29960,GnomAD)
G==0369 (10763/29118,TOPMED)
G==0324 (1621/5008,1000G)
G==0212 (816/3854,ALSPAC)
G==0213 (789/3708,TWINSUK)
chr18:76046148 (GRCh38.p7) (18q23)
AD
GWASdb2
1   publication(s)
See rs on genome
7 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 18NC_000018.10:g.76046148G>A
GRCh37.p13 chr 18NC_000018.9:g.73758103G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.607A=0.393
1000GenomesAmericanSub694G=0.230A=0.770
1000GenomesEast AsianSub1008G=0.286A=0.714
1000GenomesEuropeSub1006G=0.193A=0.807
1000GenomesGlobalStudy-wide5008G=0.324A=0.676
1000GenomesSouth AsianSub978G=0.180A=0.820
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.212A=0.788
The Genome Aggregation DatabaseAfricanSub8716G=0.539A=0.461
The Genome Aggregation DatabaseAmericanSub838G=0.230A=0.770
The Genome Aggregation DatabaseEast AsianSub1618G=0.286A=0.714
The Genome Aggregation DatabaseEuropeSub18486G=0.215A=0.784
The Genome Aggregation DatabaseGlobalStudy-wide29960G=0.312A=0.687
The Genome Aggregation DatabaseOtherSub302G=0.140A=0.860
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.369A=0.630
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.213A=0.787
PMID Title Author Journal
24277619ALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural Chinese sample.Quillen EEAm J Med Genet B Neuropsychiatr Genet

P-Value

SNP ID p-value Traits Study
rs48911120.000205alcohol dependence24277619

eQTL of rs4891112 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 rs4891112 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 )
chr187376284873763234E0714745
chr187375255373753170E081-4933
chr187375397573754047E081-4056
chr187376426773764394E0816164
chr187376447873764678E0816375
chr187376284873763234E0824745
chr187376332473764158E0825221