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rs4276227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 1.5x risk
(C;T) 1.2x risk
(T;T) 0 normal
ReferenceGRCh38 38.1/141
Chromosome3
Position32289194
GeneCMTM8
is asnp
is mentioned by
dbSNPrs4276227
ebirs4276227
HLIrs4276227
Exacrs4276227
Varsomers4276227
Maprs4276227
PheGenIrs4276227
hapmaprs4276227
1000 genomesrs4276227
hgdprs4276227
ensemblrs4276227
gopubmedrs4276227
geneviewrs4276227
scholarrs4276227
googlers4276227
pharmgkbrs4276227
gwascentralrs4276227
openSNPrs4276227
23andMers4276227
23andMe allrs4276227
SNP Nexus

SNPshotrs4276227
SNPdbers4276227
MSV3drs4276227
GWAS Ctlgrs4276227
GMAF0.3191
Max Magnitude0
? (C;C) (C;T) (T;T) 28
rs4276227 has been reported in a large study to be associated with bipolar disorder.

The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.2 (CI 0.99-1.46), and for homozygotes, 1.49 (CI 1.23-1.81). [PMID 17554300OA-icon.png]


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