rs4307816

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0166 (4976/29938,GnomAD)
G=0213 (6223/29118,TOPMED)
G=0161 (807/5008,1000G)
G=0107 (411/3854,ALSPAC)
G=0104 (384/3708,TWINSUK)
chr13:87077997 (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.87077997A>G
GRCh37.p13 chr 13NC_000013.10:g.87730252A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.613G=0.387
1000GenomesAmericanSub694A=0.890G=0.110
1000GenomesEast AsianSub1008A=0.970G=0.030
1000GenomesEuropeSub1006A=0.906G=0.094
1000GenomesGlobalStudy-wide5008A=0.839G=0.161
1000GenomesSouth AsianSub978A=0.900G=0.100
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.893G=0.107
The Genome Aggregation DatabaseAfricanSub8708A=0.633G=0.367
The Genome Aggregation DatabaseAmericanSub838A=0.920G=0.080
The Genome Aggregation DatabaseEast AsianSub1620A=0.954G=0.046
The Genome Aggregation DatabaseEuropeSub18470A=0.913G=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29938A=0.833G=0.166
The Genome Aggregation DatabaseOtherSub302A=0.840G=0.160
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.786G=0.213
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=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
rs43078167.83E-05alcohol consumption23743675

eQTL of rs4307816 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr13:87730252SLITRK5ENSG00000165300.6A>G7.2166e-3-594618Cerebellar_Hemisphere

meQTL of rs4307816 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.