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rs1344484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 normal
(C;T) 1.2x risk
(T;T) 1.5x risk
ReferenceGRCh38 38.1/141
Chromosome16
Position52878387
is asnp
is mentioned by
dbSNPrs1344484
ebirs1344484
HLIrs1344484
Exacrs1344484
Varsomers1344484
Maprs1344484
PheGenIrs1344484
hapmaprs1344484
1000 genomesrs1344484
hgdprs1344484
ensemblrs1344484
gopubmedrs1344484
geneviewrs1344484
scholarrs1344484
googlers1344484
pharmgkbrs1344484
gwascentralrs1344484
openSNPrs1344484
23andMers1344484
23andMe allrs1344484
SNP Nexus

SNPshotrs1344484
SNPdbers1344484
MSV3drs1344484
GWAS Ctlgrs1344484
GMAF0.4784
Max Magnitude0
? (C;C) (C;T) (T;T) 28
rs1344484 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 1.24 (CI 1.03-1.48), and for homozygotes, 1.52 (CI 1.27-1.82). [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 0.000002
Odds Ratio None None

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