rs9524427

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0087 (2618/29954,GnomAD)
A=0096 (2818/29118,TOPMED)
A=0079 (397/5008,1000G)
A=0104 (402/3854,ALSPAC)
A=0103 (382/3708,TWINSUK)
chr13:87062435 (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.87062435G>A
GRCh37.p13 chr 13NC_000013.10:g.87714690G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.902A=0.098
1000GenomesAmericanSub694G=0.930A=0.070
1000GenomesEast AsianSub1008G=0.970A=0.030
1000GenomesEuropeSub1006G=0.907A=0.093
1000GenomesGlobalStudy-wide5008G=0.921A=0.079
1000GenomesSouth AsianSub978G=0.900A=0.100
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.896A=0.104
The Genome Aggregation DatabaseAfricanSub8718G=0.901A=0.099
The Genome Aggregation DatabaseAmericanSub838G=0.940A=0.060
The Genome Aggregation DatabaseEast AsianSub1618G=0.955A=0.045
The Genome Aggregation DatabaseEuropeSub18478G=0.914A=0.085
The Genome Aggregation DatabaseGlobalStudy-wide29954G=0.912A=0.087
The Genome Aggregation DatabaseOtherSub302G=0.850A=0.150
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.903A=0.096
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.897A=0.103
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
rs95244270.000132alcohol consumption23743675

eQTL of rs9524427 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87714690SLITRK5ENSG00000165300.6G>A7.2166e-3-610180Cerebellar_Hemisphere

meQTL of rs9524427 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.