rs9524428

Homo sapiens
T>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0158 (4758/29952,GnomAD)
A=0204 (5960/29118,TOPMED)
A=0157 (785/5008,1000G)
A=0106 (410/3854,ALSPAC)
A=0103 (383/3708,TWINSUK)
chr13:87062874 (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.87062874T>A
GRCh37.p13 chr 13NC_000013.10:g.87715129T>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.628A=0.372
1000GenomesAmericanSub694T=0.900A=0.100
1000GenomesEast AsianSub1008T=0.970A=0.030
1000GenomesEuropeSub1006T=0.906A=0.094
1000GenomesGlobalStudy-wide5008T=0.843A=0.157
1000GenomesSouth AsianSub978T=0.900A=0.100
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.894A=0.106
The Genome Aggregation DatabaseAfricanSub8706T=0.657A=0.343
The Genome Aggregation DatabaseAmericanSub838T=0.930A=0.070
The Genome Aggregation DatabaseEast AsianSub1618T=0.955A=0.045
The Genome Aggregation DatabaseEuropeSub18490T=0.913A=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29952T=0.841A=0.158
The Genome Aggregation DatabaseOtherSub300T=0.850A=0.150
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.795A=0.204
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=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
rs95244280.000125alcohol consumption23743675

eQTL of rs9524428 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87715129SLITRK5ENSG00000165300.6T>A7.2166e-3-609741Cerebellar_Hemisphere

meQTL of rs9524428 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.