rs7328552

Homo sapiens
G>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0144 (4307/29864,GnomAD)
T=0182 (5304/29118,TOPMED)
T=0144 (722/5008,1000G)
T=0106 (407/3854,ALSPAC)
T=0102 (378/3708,TWINSUK)
chr13:87055687 (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.87055687G>T
GRCh37.p13 chr 13NC_000013.10:g.87707942G>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.672T=0.328
1000GenomesAmericanSub694G=0.910T=0.090
1000GenomesEast AsianSub1008G=0.970T=0.030
1000GenomesEuropeSub1006G=0.906T=0.094
1000GenomesGlobalStudy-wide5008G=0.856T=0.144
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 DatabaseAfricanSub8700G=0.708T=0.292
The Genome Aggregation DatabaseAmericanSub828G=0.930T=0.070
The Genome Aggregation DatabaseEast AsianSub1618G=0.955T=0.045
The Genome Aggregation DatabaseEuropeSub18418G=0.913T=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29864G=0.855T=0.144
The Genome Aggregation DatabaseOtherSub300G=0.840T=0.160
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.817T=0.182
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.898T=0.102
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
rs73285520.000115alcohol consumption23743675

eQTL of rs7328552 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87707942SLITRK5ENSG00000165300.6G>T7.2166e-3-616928Cerebellar_Hemisphere

meQTL of rs7328552 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.