rs9516391

Homo sapiens
A>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0158 (4757/29938,GnomAD)
C=0204 (5960/29118,TOPMED)
C=0157 (785/5008,1000G)
C=0106 (410/3854,ALSPAC)
C=0103 (383/3708,TWINSUK)
chr13:87065008 (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.87065008A>C
GRCh37.p13 chr 13NC_000013.10:g.87717263A>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.628C=0.372
1000GenomesAmericanSub694A=0.900C=0.100
1000GenomesEast AsianSub1008A=0.970C=0.030
1000GenomesEuropeSub1006A=0.906C=0.094
1000GenomesGlobalStudy-wide5008A=0.843C=0.157
1000GenomesSouth AsianSub978A=0.900C=0.100
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.894C=0.106
The Genome Aggregation DatabaseAfricanSub8694A=0.657C=0.343
The Genome Aggregation DatabaseAmericanSub836A=0.930C=0.070
The Genome Aggregation DatabaseEast AsianSub1620A=0.954C=0.046
The Genome Aggregation DatabaseEuropeSub18490A=0.913C=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29938A=0.841C=0.158
The Genome Aggregation DatabaseOtherSub298A=0.850C=0.150
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.795C=0.204
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.897C=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
rs95163910.000113alcohol consumption23743675

eQTL of rs9516391 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87717263SLITRK5ENSG00000165300.6A>C7.2166e-3-607607Cerebellar_Hemisphere

meQTL of rs9516391 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.