rs9524592

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0066 (2002/29968,GnomAD)
G=0067 (1976/29118,TOPMED)
G=0061 (304/5008,1000G)
G=0105 (403/3854,ALSPAC)
G=0104 (386/3708,TWINSUK)
chr13:87102225 (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.87102225A>G
GRCh37.p13 chr 13NC_000013.10:g.87754480A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.982G=0.018
1000GenomesAmericanSub694A=0.940G=0.060
1000GenomesEast AsianSub1008A=0.968G=0.032
1000GenomesEuropeSub1006A=0.908G=0.092
1000GenomesGlobalStudy-wide5008A=0.939G=0.061
1000GenomesSouth AsianSub978A=0.890G=0.110
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.895G=0.105
The Genome Aggregation DatabaseAfricanSub8726A=0.972G=0.028
The Genome Aggregation DatabaseAmericanSub838A=0.940G=0.060
The Genome Aggregation DatabaseEast AsianSub1618A=0.954G=0.046
The Genome Aggregation DatabaseEuropeSub18484A=0.914G=0.085
The Genome Aggregation DatabaseGlobalStudy-wide29968A=0.933G=0.066
The Genome Aggregation DatabaseOtherSub302A=0.840G=0.160
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.932G=0.067
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.896G=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
rs95245920.00013alcohol consumption23743675

eQTL of rs9524592 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87754480SLITRK5ENSG00000165300.6A>G7.2166e-3-570390Cerebellar_Hemisphere

meQTL of rs9524592 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 )
chr138778075187780970E07026271
chr138778099087781070E07026510
chr138778113987781194E07026659
chr138778136187781523E07026881
chr138778160987781698E07027129
chr138778189787782225E07027417
chr138778224887782420E07027768
chr138778273087782844E07028250
chr138778399687784117E07029516