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rs10982256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 1.5x risk
(C;T) 1.3x risk
(G;G) 0
(T;T) normal
ReferenceGRCh38 38.1/141
Chromosome9
Position114498554
GeneDFNB31
is asnp
is mentioned by
dbSNPrs10982256
ebirs10982256
HLIrs10982256
Exacrs10982256
Varsomers10982256
Maprs10982256
PheGenIrs10982256
hapmaprs10982256
1000 genomesrs10982256
hgdprs10982256
ensemblrs10982256
gopubmedrs10982256
geneviewrs10982256
scholarrs10982256
googlers10982256
pharmgkbrs10982256
gwascentralrs10982256
openSNPrs10982256
23andMers10982256
23andMe allrs10982256
SNP Nexus

SNPshotrs10982256
SNPdbers10982256
MSV3drs10982256
GWAS Ctlgrs10982256
GMAF0.4008
Max Magnitude0
? (C;C) (C;T) (T;T) 28
rs10982256 has been reported in a large study to be associated with bipolar disorder.

The risk allele (oriented to the dbSNP entry) is (T); the odds ratio associated with heterozygotes is 1.26 (CI 1.08-1.47), and for homozygotes, 1.47 (CI 1.24-1.74). [PMID 17554300OA-icon.png]

GWAS snp
PMID [PMID 21254220OA-icon.png]
Trait
Title Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Risk Allele
P-val 0.000009
Odds Ratio None None


[PMID 18421293OA-icon.png] Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement.


[PMID 19308021OA-icon.png] Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort.