rs9516565

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0065 (1960/29984,GnomAD)
A=0066 (1930/29118,TOPMED)
A=0060 (300/5008,1000G)
A=0105 (403/3854,ALSPAC)
A=0104 (386/3708,TWINSUK)
chr13:87166282 (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.87166282G>A
GRCh37.p13 chr 13NC_000013.10:g.87818537G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.986A=0.014
1000GenomesAmericanSub694G=0.940A=0.060
1000GenomesEast AsianSub1008G=0.968A=0.032
1000GenomesEuropeSub1006G=0.908A=0.092
1000GenomesGlobalStudy-wide5008G=0.940A=0.060
1000GenomesSouth AsianSub978G=0.880A=0.120
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.895A=0.105
The Genome Aggregation DatabaseAfricanSub8730G=0.976A=0.024
The Genome Aggregation DatabaseAmericanSub838G=0.950A=0.050
The Genome Aggregation DatabaseEast AsianSub1620G=0.953A=0.047
The Genome Aggregation DatabaseEuropeSub18494G=0.914A=0.085
The Genome Aggregation DatabaseGlobalStudy-wide29984G=0.934A=0.065
The Genome Aggregation DatabaseOtherSub302G=0.850A=0.150
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.933A=0.066
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
rs95165650.000171alcohol consumption23743675

eQTL of rs9516565 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87818537SLITRK5ENSG00000165300.6G>A7.2166e-3-506333Cerebellar_Hemisphere

meQTL of rs9516565 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 )
chr138778075187780970E070-37567
chr138778099087781070E070-37467
chr138778113987781194E070-37343
chr138778136187781523E070-37014
chr138778160987781698E070-36839
chr138778189787782225E070-36312
chr138778224887782420E070-36117
chr138778273087782844E070-35693
chr138778399687784117E070-34420