Rs2953145

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs2953145
hapmaprs2953145
hgdprs2953145
ensemblrs2953145
gopubmedrs2953145
scholarrs2953145
googlers2953145
pharmgkbrs2953145
hgvbaseg2prs2953145
medrefsnprs2953145
23andMers2953145
SNP Nexus

GeneRNPEPL1
Chromosome2
Orientationminus
Position241164268
GenotypeEffect
rs2953145(G;G)2.1x risk
rs2953145(C;G)1.8x risk
rs2953145(C;C)normal


Genotypes Magnitude Summary
Rs2953145(C;C) 00 normal
Rs2953145(C;G) 1.8x risk
Rs2953145(G;G) 2.1x risk

rs2953145 has been reported in a large study to be associated with bipolar disorder.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.84 (CI 1.31-2.58), and for homozygotes, 2.14 (CI 1.53-2.98). [PMID 17554300]

? (C;C) (C;G) (G;G)
GWAS
SNP rs2953145
PubMedID [PMID 17554300]
Condition Bipolar disorder
Gene NR
Risk Allele C
pValue 7.00E-006
OR 1.84
95% CI 1.31-2.58


PharmGKBPA162356651
Name
AnnotationGWAS Results: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Initial Sample Size: 1,868 cases, 2,938 controls; Replication Sample Size: NR; Risk Allele: rs2953145-C). This variant is associated with bipolar disorder.
GeneRNPEPL1
Featue
EvidencePubMed ID:17554300; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesBipolar Disorder
Curation LevelNon-Curated