rs12901215

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0232 (6929/29870,GnomAD)
A=0233 (6797/29118,TOPMED)
A=0169 (846/5008,1000G)
A=0303 (1166/3854,ALSPAC)
A=0301 (1116/3708,TWINSUK)
chr15:38700692 (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.38700692G>A
GRCh37.p13 chr 15NC_000015.9:g.38992893G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.852A=0.148
1000GenomesAmericanSub694G=0.750A=0.250
1000GenomesEast AsianSub1008G=0.967A=0.033
1000GenomesEuropeSub1006G=0.749A=0.251
1000GenomesGlobalStudy-wide5008G=0.831A=0.169
1000GenomesSouth AsianSub978G=0.800A=0.200
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.697A=0.303
The Genome Aggregation DatabaseAfricanSub8680G=0.828A=0.172
The Genome Aggregation DatabaseAmericanSub838G=0.760A=0.240
The Genome Aggregation DatabaseEast AsianSub1620G=0.972A=0.028
The Genome Aggregation DatabaseEuropeSub18430G=0.722A=0.277
The Genome Aggregation DatabaseGlobalStudy-wide29870G=0.768A=0.232
The Genome Aggregation DatabaseOtherSub302G=0.740A=0.260
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.766A=0.233
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.699A=0.301
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
rs129012154.38E-07alcohol dependence23089632

eQTL of rs12901215 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 rs12901215 in Fetal Brain

Probe ID Position Gene beta p-value
cg21039679chr15:38989738C15orf53-0.02562029628647616.4824e-14

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 )
chr153896065238961725E068-31168
chr153896065238961725E069-31168
chr153896065238961725E070-31168
chr153900002839001434E0817135
chr153900646639007349E08113573
chr153896051838960573E082-32320
chr153896065238961725E082-31168