rs9516421

Homo sapiens
G>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0152 (4564/29928,GnomAD)
T=0193 (5647/29118,TOPMED)
T=0150 (750/5008,1000G)
T=0106 (410/3854,ALSPAC)
T=0104 (386/3708,TWINSUK)
chr13:87079343 (GRCh38.p7) (13q31.1)
AD
GWASdb2
1   publication(s)
See rs on genome
4 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.87079343G>T
GRCh37.p13 chr 13NC_000013.10:g.87731598G>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.652T=0.348
1000GenomesAmericanSub694G=0.900T=0.100
1000GenomesEast AsianSub1008G=0.970T=0.030
1000GenomesEuropeSub1006G=0.906T=0.094
1000GenomesGlobalStudy-wide5008G=0.850T=0.150
1000GenomesSouth AsianSub978G=0.900T=0.100
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.894T=0.106
The Genome Aggregation DatabaseAfricanSub8688G=0.678T=0.322
The Genome Aggregation DatabaseAmericanSub838G=0.930T=0.070
The Genome Aggregation DatabaseEast AsianSub1618G=0.956T=0.044
The Genome Aggregation DatabaseEuropeSub18484G=0.913T=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29928G=0.847T=0.152
The Genome Aggregation DatabaseOtherSub300G=0.850T=0.150
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.806T=0.193
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.896T=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
rs95164210.000106alcohol consumption23743675

eQTL of rs9516421 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87731598SLITRK5ENSG00000165300.6G>T7.2166e-3-593272Cerebellar_Hemisphere

meQTL of rs9516421 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 )
chr138778075187780970E07049153
chr138778099087781070E07049392
chr138778113987781194E07049541
chr138778136187781523E07049763