rs36094159

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0228 (6828/29902,GnomAD)
A=0228 (6651/29118,TOPMED)
A=0166 (832/5008,1000G)
A=0292 (1125/3854,ALSPAC)
A=0290 (1077/3708,TWINSUK)
chr15:38706194 (GRCh38.p7) (15q14)
AD
GWASdb2
1   publication(s)
See rs on genome
7 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 15NC_000015.10:g.38706194G>A
GRCh37.p13 chr 15NC_000015.9:g.38998395G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.850A=0.150
1000GenomesAmericanSub694G=0.760A=0.240
1000GenomesEast AsianSub1008G=0.970A=0.030
1000GenomesEuropeSub1006G=0.752A=0.248
1000GenomesGlobalStudy-wide5008G=0.834A=0.166
1000GenomesSouth AsianSub978G=0.810A=0.190
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.708A=0.292
The Genome Aggregation DatabaseAfricanSub8700G=0.822A=0.178
The Genome Aggregation DatabaseAmericanSub838G=0.760A=0.240
The Genome Aggregation DatabaseEast AsianSub1616G=0.971A=0.029
The Genome Aggregation DatabaseEuropeSub18446G=0.731A=0.268
The Genome Aggregation DatabaseGlobalStudy-wide29902G=0.771A=0.228
The Genome Aggregation DatabaseOtherSub302G=0.750A=0.250
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.771A=0.228
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.710A=0.290
PMID Title Author Journal
23089632A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53.Wang JCMol Psychiatry

P-Value

SNP ID p-value Traits Study
rs360941596.94E-07alcohol dependence23089632

eQTL of rs36094159 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 rs36094159 in Fetal Brain

Probe ID Position Gene beta p-value
cg21039679chr15:38989738C15orf53-0.02362836806952721.3452e-12

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 )
chr153896065238961725E068-36670
chr153896065238961725E069-36670
chr153896065238961725E070-36670
chr153900002839001434E0811633
chr153900646639007349E0818071
chr153896051838960573E082-37822
chr153896065238961725E082-36670