rs9516432

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0068 (2043/29932,GnomAD)
A=0070 (2040/29118,TOPMED)
A=0062 (313/5008,1000G)
A=0104 (400/3854,ALSPAC)
A=0104 (386/3708,TWINSUK)
chr13:87090028 (GRCh38.p7) (13q31.1)
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.87090028G>A
GRCh37.p13 chr 13NC_000013.10:g.87742283G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.976A=0.024
1000GenomesAmericanSub694G=0.940A=0.060
1000GenomesEast AsianSub1008G=0.968A=0.032
1000GenomesEuropeSub1006G=0.908A=0.092
1000GenomesGlobalStudy-wide5008G=0.938A=0.062
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 DatabaseAfricanSub8718G=0.967A=0.033
The Genome Aggregation DatabaseAmericanSub836G=0.940A=0.060
The Genome Aggregation DatabaseEast AsianSub1610G=0.953A=0.047
The Genome Aggregation DatabaseEuropeSub18466G=0.914A=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29932G=0.931A=0.068
The Genome Aggregation DatabaseOtherSub302G=0.850A=0.150
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.929A=0.070
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
rs95164320.000129alcohol consumption23743675

eQTL of rs9516432 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87742283SLITRK5ENSG00000165300.6G>A7.2166e-3-582587Cerebellar_Hemisphere

meQTL of rs9516432 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 )
chr138778075187780970E07038468
chr138778099087781070E07038707
chr138778113987781194E07038856
chr138778136187781523E07039078
chr138778160987781698E07039326
chr138778189787782225E07039614
chr138778224887782420E07039965
chr138778273087782844E07040447
chr138778399687784117E07041713