rs9883805

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0164 (4928/29952,GnomAD)
G=0183 (5343/29118,TOPMED)
G=0195 (975/5008,1000G)
G=0101 (388/3854,ALSPAC)
G=0106 (393/3708,TWINSUK)
chr3:110242347 (GRCh38.p7) (3q13.13)
AD
GWASdb2
2   publication(s)
See rs on genome
6 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.110242347A>G
GRCh37.p13 chr 3NC_000003.11:g.109961194A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.677G=0.323
1000GenomesAmericanSub694A=0.860G=0.140
1000GenomesEast AsianSub1008A=0.753G=0.247
1000GenomesEuropeSub1006A=0.904G=0.096
1000GenomesGlobalStudy-wide5008A=0.805G=0.195
1000GenomesSouth AsianSub978A=0.890G=0.110
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.899G=0.101
The Genome Aggregation DatabaseAfricanSub8706A=0.705G=0.295
The Genome Aggregation DatabaseAmericanSub838A=0.860G=0.140
The Genome Aggregation DatabaseEast AsianSub1614A=0.745G=0.255
The Genome Aggregation DatabaseEuropeSub18492A=0.902G=0.097
The Genome Aggregation DatabaseGlobalStudy-wide29952A=0.835G=0.164
The Genome Aggregation DatabaseOtherSub302A=0.920G=0.080
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.816G=0.183
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.894G=0.106
PMID Title Author Journal
21302341Replicated genome wide association for dependence on illegal substances: genomic regions identified by overlapping clusters of nominally positive SNPs.Drgon TAm J Med Genet B Neuropsychiatr Genet
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
rs98838050.000281alcohol consumption (maxi-drinks)24277619

eQTL of rs9883805 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 rs9883805 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 )
chr3109917656109917744E070-43450
chr3110001899110002049E07040705
chr3109955692109956302E081-4892
chr3110001899110002049E08140705
chr3109955692109956302E082-4892
chr3110002429110002610E08241235