rs9584218

Homo sapiens
G>C
None
Check p-value
SNV (Single Nucleotide Variation)
C=0158 (4751/29908,GnomAD)
C=0204 (5960/29118,TOPMED)
C=0157 (785/5008,1000G)
C=0106 (410/3854,ALSPAC)
C=0103 (383/3708,TWINSUK)
chr13:87070020 (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.87070020G>C
GRCh37.p13 chr 13NC_000013.10:g.87722275G>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.628C=0.372
1000GenomesAmericanSub694G=0.900C=0.100
1000GenomesEast AsianSub1008G=0.970C=0.030
1000GenomesEuropeSub1006G=0.906C=0.094
1000GenomesGlobalStudy-wide5008G=0.843C=0.157
1000GenomesSouth AsianSub978G=0.900C=0.100
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.894C=0.106
The Genome Aggregation DatabaseAfricanSub8700G=0.658C=0.342
The Genome Aggregation DatabaseAmericanSub830G=0.930C=0.070
The Genome Aggregation DatabaseEast AsianSub1620G=0.954C=0.046
The Genome Aggregation DatabaseEuropeSub18456G=0.913C=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29908G=0.841C=0.158
The Genome Aggregation DatabaseOtherSub302G=0.840C=0.160
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.795C=0.204
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.897C=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
rs95842180.000112alcohol consumption23743675

eQTL of rs9584218 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87722275SLITRK5ENSG00000165300.6G>C7.2166e-3-602595Cerebellar_Hemisphere

meQTL of rs9584218 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.