rs9516574

Homo sapiens
C>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0078 (2358/29938,GnomAD)
G=0086 (2522/29118,TOPMED)
G=0073 (365/5008,1000G)
G=0105 (403/3854,ALSPAC)
G=0104 (385/3708,TWINSUK)
chr13:87168105 (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.87168105C>G
GRCh37.p13 chr 13NC_000013.10:g.87820360C>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.942G=0.058
1000GenomesAmericanSub694C=0.930G=0.070
1000GenomesEast AsianSub1008C=0.968G=0.032
1000GenomesEuropeSub1006C=0.908G=0.092
1000GenomesGlobalStudy-wide5008C=0.927G=0.073
1000GenomesSouth AsianSub978C=0.880G=0.120
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.895G=0.105
The Genome Aggregation DatabaseAfricanSub8708C=0.931G=0.069
The Genome Aggregation DatabaseAmericanSub836C=0.940G=0.060
The Genome Aggregation DatabaseEast AsianSub1622C=0.953G=0.047
The Genome Aggregation DatabaseEuropeSub18472C=0.914G=0.085
The Genome Aggregation DatabaseGlobalStudy-wide29938C=0.921G=0.078
The Genome Aggregation DatabaseOtherSub300C=0.840G=0.160
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.913G=0.086
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.896G=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
rs95165740.000171alcohol consumption23743675

eQTL of rs9516574 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87820360SLITRK5ENSG00000165300.6C>G7.2166e-3-504510Cerebellar_Hemisphere

meQTL of rs9516574 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 )
chr138778075187780970E070-39390
chr138778099087781070E070-39290
chr138778113987781194E070-39166
chr138778136187781523E070-38837
chr138778160987781698E070-38662
chr138778189787782225E070-38135
chr138778224887782420E070-37940
chr138778273087782844E070-37516
chr138778399687784117E070-36243