rs9523979

Homo sapiens
G>A / G>C
None
Check p-value
SNV (Single Nucleotide Variation)
A=0083 (2505/29924,GnomAD)
A=0093 (2725/29118,TOPMED)
A=0073 (368/5008,1000G)
A=0105 (405/3854,ALSPAC)
A=0102 (380/3708,TWINSUK)
chr13:86956227 (GRCh38.p7) (13q31.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.86956227G>A
GRCh38.p7 chr 13NC_000013.11:g.86956227G>C
GRCh37.p13 chr 13NC_000013.10:g.87608482G>A
GRCh37.p13 chr 13NC_000013.10:g.87608482G>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.926A=0.074
1000GenomesAmericanSub694G=0.930A=0.070
1000GenomesEast AsianSub1008G=0.965A=0.035
1000GenomesEuropeSub1006G=0.908A=0.092
1000GenomesGlobalStudy-wide5008G=0.927A=0.073
1000GenomesSouth AsianSub978G=0.900A=0.100
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.895A=0.105
The Genome Aggregation DatabaseAfricanSub8704G=0.914C=0.000
The Genome Aggregation DatabaseAmericanSub836G=0.940C=0.00,
The Genome Aggregation DatabaseEast AsianSub1620G=0.951C=0.000
The Genome Aggregation DatabaseEuropeSub18462G=0.913C=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29924G=0.916C=0.000
The Genome Aggregation DatabaseOtherSub302G=0.850C=0.00,
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.906A=0.093
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.898A=0.102
PMID Title Author Journal
23743675A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.Kapoor MHum Genet

P-Value

SNP ID p-value Traits Study
rs95239799.76E-05alcohol consumption23743675

eQTL of rs9523979 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87608482SLITRK5ENSG00000165300.6G>A7.2166e-3-716388Cerebellar_Hemisphere

meQTL of rs9523979 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.