rs13406625

Homo sapiens
T>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0089 (2591/29116,TOPMED)
C=0087 (2082/23674,GnomAD)
C=0096 (482/5008,1000G)
C=0042 (160/3854,ALSPAC)
C=0043 (158/3708,TWINSUK)
chr2:56494872 (GRCh38.p7) (2p16.1)
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.56494872T>C
GRCh37.p13 chr 2NC_000002.11:g.56722007T>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.831C=0.169
1000GenomesAmericanSub694T=0.880C=0.120
1000GenomesEast AsianSub1008T=0.924C=0.076
1000GenomesEuropeSub1006T=0.953C=0.047
1000GenomesGlobalStudy-wide5008T=0.904C=0.096
1000GenomesSouth AsianSub978T=0.950C=0.050
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.958C=0.042
The Genome Aggregation DatabaseAfricanSub7028T=0.840C=0.160
The Genome Aggregation DatabaseAmericanSub686T=0.830C=0.170
The Genome Aggregation DatabaseEast AsianSub1394T=0.902C=0.098
The Genome Aggregation DatabaseEuropeSub14306T=0.951C=0.048
The Genome Aggregation DatabaseGlobalStudy-wide23674T=0.912C=0.087
The Genome Aggregation DatabaseOtherSub260T=0.950C=0.050
Trans-Omics for Precision MedicineGlobalStudy-wide29116T=0.911C=0.089
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.957C=0.043
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
rs134066250.00074alcohol consumption (maxi-drinks)24277619

eQTL of rs13406625 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 rs13406625 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.