Have questions? Visit https://www.reddit.com/r/SNPedia

rs9378249

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs9378249(G;G)
Make rs9378249(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31359924
is asnp
is mentioned by
dbSNPrs9378249
ebirs9378249
HLIrs9378249
Exacrs9378249
Varsomers9378249
Maprs9378249
PheGenIrs9378249
hapmaprs9378249
1000 genomesrs9378249
hgdprs9378249
ensemblrs9378249
gopubmedrs9378249
geneviewrs9378249
scholarrs9378249
googlers9378249
pharmgkbrs9378249
gwascentralrs9378249
openSNPrs9378249
23andMers9378249
23andMe allrs9378249
SNP Nexus

SNPshotrs9378249
SNPdbers9378249
MSV3drs9378249
GWAS Ctlgrs9378249
GMAF0.07025
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 21254220OA-icon.png]
Trait
Title Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Risk Allele
P-val 1E-8
Odds Ratio None None

[PMID 21291537OA-icon.png] Evidence for somatic gene conversion and deletion in bipolar disorder, Crohn's disease, coronary artery disease, hypertension, rheumatoid arthritis, type-1 diabetes, and type-2 diabetes.