rs13271637

Homo sapiens
G>A / G>C
None
Check p-value
SNV (Single Nucleotide Variation)
A=0268 (8027/29930,GnomAD)
A=0220 (6418/29118,TOPMED)
A=0169 (845/5008,1000G)
A=0295 (1136/3854,ALSPAC)
A=0311 (1153/3708,TWINSUK)
chr8:15500300 (GRCh38.p7) (8p22)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 8NC_000008.11:g.15500300G>A
GRCh38.p7 chr 8NC_000008.11:g.15500300G>C
GRCh37.p13 chr 8NC_000008.10:g.15357809G>A
GRCh37.p13 chr 8NC_000008.10:g.15357809G>C

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.871A=0.129
1000GenomesAmericanSub694G=0.760A=0.240
1000GenomesEast AsianSub1008G=0.905A=0.095
1000GenomesEuropeSub1006G=0.706A=0.294
1000GenomesGlobalStudy-wide5008G=0.831A=0.169
1000GenomesSouth AsianSub978G=0.880A=0.120
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.705A=0.295
The Genome Aggregation DatabaseAfricanSub8706G=0.832A=0.168
The Genome Aggregation DatabaseAmericanSub838G=0.780A=0.220
The Genome Aggregation DatabaseEast AsianSub1612G=0.922A=0.078
The Genome Aggregation DatabaseEuropeSub18472G=0.664A=0.335
The Genome Aggregation DatabaseGlobalStudy-wide29930G=0.731A=0.268
The Genome Aggregation DatabaseOtherSub302G=0.800A=0.200
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.779A=0.220
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.689A=0.311
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs132716370.00014alcohol dependence(early age of onset)20201924
rs132716370.00065alcohol dependence20201924

eQTL of rs13271637 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs13271637 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.