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rs5907577

From SNPedia

Orientationplus
Stabilizedplus
Make rs5907577(C;C)
Make rs5907577(C;T)
Make rs5907577(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position140084524
is asnp
is mentioned by
dbSNPrs5907577
ebirs5907577
HLIrs5907577
Exacrs5907577
Varsomers5907577
Maprs5907577
PheGenIrs5907577
hapmaprs5907577
1000 genomesrs5907577
hgdprs5907577
ensemblrs5907577
gopubmedrs5907577
geneviewrs5907577
scholarrs5907577
googlers5907577
pharmgkbrs5907577
gwascentralrs5907577
openSNPrs5907577
23andMers5907577
23andMe allrs5907577
SNP Nexus

SNPshotrs5907577
SNPdbers5907577
MSV3drs5907577
GWAS Ctlgrs5907577
GMAF0.2122
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19488044OA-icon.png] Associated with bipolar disorder in individuals of European ancestry.
GWAS snp
PMID [PMID 20889312]
Trait Bipolar disorder and schizophrenia
Title A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
Risk Allele
P-val 5E-6
Odds Ratio 1.27 [NR]