rs9516389

Homo sapiens
T>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0159 (4775/29968,GnomAD)
G=0204 (5963/29118,TOPMED)
G=0157 (785/5008,1000G)
G=0106 (410/3854,ALSPAC)
G=0103 (383/3708,TWINSUK)
chr13:87064491 (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.87064491T>G
GRCh37.p13 chr 13NC_000013.10:g.87716746T>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.628G=0.372
1000GenomesAmericanSub694T=0.900G=0.100
1000GenomesEast AsianSub1008T=0.970G=0.030
1000GenomesEuropeSub1006T=0.906G=0.094
1000GenomesGlobalStudy-wide5008T=0.843G=0.157
1000GenomesSouth AsianSub978T=0.900G=0.100
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.894G=0.106
The Genome Aggregation DatabaseAfricanSub8720T=0.657G=0.343
The Genome Aggregation DatabaseAmericanSub834T=0.930G=0.070
The Genome Aggregation DatabaseEast AsianSub1620T=0.955G=0.045
The Genome Aggregation DatabaseEuropeSub18492T=0.913G=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29968T=0.840G=0.159
The Genome Aggregation DatabaseOtherSub302T=0.840G=0.160
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.795G=0.204
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.897G=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
rs95163890.00011alcohol consumption23743675

eQTL of rs9516389 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87716746SLITRK5ENSG00000165300.6T>G7.2166e-3-608124Cerebellar_Hemisphere

meQTL of rs9516389 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.