rs12899449

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0227 (6802/29952,GnomAD)
G=0229 (6695/29118,TOPMED)
G=0168 (839/5008,1000G)
G=0298 (1150/3854,ALSPAC)
G=0295 (1094/3708,TWINSUK)
chr15:38703290 (GRCh38.p7) (15q14)
AD
GWASdb2
4   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.38703290A>G
GRCh37.p13 chr 15NC_000015.9:g.38995491A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.856G=0.144
1000GenomesAmericanSub694A=0.750G=0.250
1000GenomesEast AsianSub1008A=0.968G=0.032
1000GenomesEuropeSub1006A=0.750G=0.250
1000GenomesGlobalStudy-wide5008A=0.832G=0.168
1000GenomesSouth AsianSub978A=0.800G=0.200
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.702G=0.298
The Genome Aggregation DatabaseAfricanSub8714A=0.834G=0.166
The Genome Aggregation DatabaseAmericanSub834A=0.760G=0.240
The Genome Aggregation DatabaseEast AsianSub1620A=0.972G=0.028
The Genome Aggregation DatabaseEuropeSub18482A=0.728G=0.271
The Genome Aggregation DatabaseGlobalStudy-wide29952A=0.772G=0.227
The Genome Aggregation DatabaseOtherSub302A=0.730G=0.270
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.770G=0.229
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.705G=0.295
PMID Title Author Journal
18711365Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.Ferreira MANat Genet
22212596Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.Gamazon ERMol Psychiatry
23871474A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.Bramon EBiol Psychiatry
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
rs128994491.26E-05alcohol dependence23089632

eQTL of rs12899449 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 rs12899449 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 )
chr153896065238961725E068-33766
chr153896065238961725E069-33766
chr153896065238961725E070-33766
chr153900002839001434E0814537
chr153900646639007349E08110975
chr153896051838960573E082-34918
chr153896065238961725E082-33766