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rs5990417

From SNPedia

Orientationplus
Stabilizedplus
Make rs5990417(C;C)
Make rs5990417(C;T)
Make rs5990417(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position95824871
is asnp
is mentioned by
dbSNPrs5990417
ebirs5990417
HLIrs5990417
Exacrs5990417
Varsomers5990417
Maprs5990417
PheGenIrs5990417
hapmaprs5990417
1000 genomesrs5990417
hgdprs5990417
ensemblrs5990417
gopubmedrs5990417
geneviewrs5990417
scholarrs5990417
googlers5990417
pharmgkbrs5990417
gwascentralrs5990417
openSNPrs5990417
23andMers5990417
23andMe allrs5990417
SNP Nexus

SNPshotrs5990417
SNPdbers5990417
MSV3drs5990417
GWAS Ctlgrs5990417
GMAF0.2092
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20038947OA-icon.png]
Trait Major depressive disorder (broad)
Title Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies
Risk Allele T
P-val 0.000006
Odds Ratio 1.23 [NR]