rs9516435

Homo sapiens
A>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0123 (3700/29906,GnomAD)
T=0152 (4451/29118,TOPMED)
T=0118 (591/5008,1000G)
T=0104 (400/3854,ALSPAC)
T=0104 (386/3708,TWINSUK)
chr13:87091321 (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.87091321A>T
GRCh37.p13 chr 13NC_000013.10:g.87743576A>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.783T=0.217
1000GenomesAmericanSub694A=0.910T=0.090
1000GenomesEast AsianSub1008A=0.968T=0.032
1000GenomesEuropeSub1006A=0.906T=0.094
1000GenomesGlobalStudy-wide5008A=0.882T=0.118
1000GenomesSouth AsianSub978A=0.880T=0.120
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.896T=0.104
The Genome Aggregation DatabaseAfricanSub8704A=0.779T=0.221
The Genome Aggregation DatabaseAmericanSub834A=0.920T=0.080
The Genome Aggregation DatabaseEast AsianSub1614A=0.954T=0.046
The Genome Aggregation DatabaseEuropeSub18454A=0.913T=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29906A=0.876T=0.123
The Genome Aggregation DatabaseOtherSub300A=0.850T=0.150
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.847T=0.152
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=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
rs95164350.000124alcohol consumption23743675

eQTL of rs9516435 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87743576SLITRK5ENSG00000165300.6A>T7.2166e-3-581294Cerebellar_Hemisphere

meQTL of rs9516435 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 )
chr138778075187780970E07037175
chr138778099087781070E07037414
chr138778113987781194E07037563
chr138778136187781523E07037785
chr138778160987781698E07038033
chr138778189787782225E07038321
chr138778224887782420E07038672
chr138778273087782844E07039154
chr138778399687784117E07040420