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rs4739466

From SNPedia

Orientationplus
Stabilizedplus
Make rs4739466(G;G)
Make rs4739466(G;T)
Make rs4739466(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position37084024
is asnp
is mentioned by
dbSNPrs4739466
dbSNP (classic)rs4739466
ClinGenrs4739466
ebirs4739466
HLIrs4739466
Exacrs4739466
Gnomadrs4739466
Varsomers4739466
LitVarrs4739466
Maprs4739466
PheGenIrs4739466
Biobankrs4739466
1000 genomesrs4739466
hgdprs4739466
ensemblrs4739466
geneviewrs4739466
scholarrs4739466
googlers4739466
pharmgkbrs4739466
gwascentralrs4739466
openSNPrs4739466
23andMers4739466
SNPshotrs4739466
SNPdbers4739466
MSV3drs4739466
GWAS Ctlgrs4739466
GMAF0.1419
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 0.000004
Odds Ratio None None