rs9524641

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0066 (1999/29960,GnomAD)
A=0067 (1972/29118,TOPMED)
A=0061 (305/5008,1000G)
A=0104 (400/3854,ALSPAC)
A=0104 (385/3708,TWINSUK)
chr13:87115606 (GRCh38.p7) (13q31.2)
AD
GWASdb2
1   publication(s)
See rs on genome
9 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.87115606G>A
GRCh37.p13 chr 13NC_000013.10:g.87767861G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.982A=0.018
1000GenomesAmericanSub694G=0.940A=0.060
1000GenomesEast AsianSub1008G=0.968A=0.032
1000GenomesEuropeSub1006G=0.908A=0.092
1000GenomesGlobalStudy-wide5008G=0.939A=0.061
1000GenomesSouth AsianSub978G=0.890A=0.110
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.896A=0.104
The Genome Aggregation DatabaseAfricanSub8720G=0.972A=0.028
The Genome Aggregation DatabaseAmericanSub838G=0.940A=0.060
The Genome Aggregation DatabaseEast AsianSub1616G=0.954A=0.046
The Genome Aggregation DatabaseEuropeSub18484G=0.914A=0.085
The Genome Aggregation DatabaseGlobalStudy-wide29960G=0.933A=0.066
The Genome Aggregation DatabaseOtherSub302G=0.840A=0.160
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.932A=0.067
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.896A=0.104
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
rs95246417.96E-05alcohol consumption23743675

eQTL of rs9524641 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87767861SLITRK5ENSG00000165300.6G>A7.2166e-3-557009Cerebellar_Hemisphere

meQTL of rs9524641 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 )
chr138778075187780970E07012890
chr138778099087781070E07013129
chr138778113987781194E07013278
chr138778136187781523E07013500
chr138778160987781698E07013748
chr138778189787782225E07014036
chr138778224887782420E07014387
chr138778273087782844E07014869
chr138778399687784117E07016135