rs160816

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0438 (13102/29910,GnomAD)
A=0466 (13592/29118,TOPMED)
A=0483 (2417/5008,1000G)
A=0368 (1417/3854,ALSPAC)
A=0365 (1352/3708,TWINSUK)
chr13:93099704 (GRCh38.p7) (13q31.3)
AD
GWASdb2
1   publication(s)
See rs on genome
3 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.93099704G>A
GRCh37.p13 chr 13NC_000013.10:g.93751957G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.400A=0.600
1000GenomesAmericanSub694G=0.420A=0.580
1000GenomesEast AsianSub1008G=0.513A=0.487
1000GenomesEuropeSub1006G=0.645A=0.355
1000GenomesGlobalStudy-wide5008G=0.517A=0.483
1000GenomesSouth AsianSub978G=0.620A=0.380
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.632A=0.368
The Genome Aggregation DatabaseAfricanSub8698G=0.424A=0.576
The Genome Aggregation DatabaseAmericanSub838G=0.410A=0.590
The Genome Aggregation DatabaseEast AsianSub1614G=0.532A=0.468
The Genome Aggregation DatabaseEuropeSub18460G=0.636A=0.363
The Genome Aggregation DatabaseGlobalStudy-wide29910G=0.562A=0.438
The Genome Aggregation DatabaseOtherSub300G=0.590A=0.410
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.533A=0.466
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.635A=0.365
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
rs1608169.2E-05alcohol consumption (maxi-drinks)24277619

eQTL of rs160816 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 rs160816 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 )
chr139372771793727913E070-24044
chr139372795593728187E070-23770
chr139372881893728868E070-23089