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rs2073831

From SNPedia

Orientationplus
Stabilizedplus
Make rs2073831(C;C)
Make rs2073831(C;T)
Make rs2073831(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position76924565
is asnp
is mentioned by
dbSNPrs2073831
ebirs2073831
HLIrs2073831
Exacrs2073831
Varsomers2073831
Maprs2073831
PheGenIrs2073831
hapmaprs2073831
1000 genomesrs2073831
hgdprs2073831
ensemblrs2073831
gopubmedrs2073831
geneviewrs2073831
scholarrs2073831
googlers2073831
pharmgkbrs2073831
gwascentralrs2073831
openSNPrs2073831
23andMers2073831
23andMe allrs2073831
SNP Nexus

SNPshotrs2073831
SNPdbers2073831
MSV3drs2073831
GWAS Ctlgrs2073831
GMAF0.3604
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20386566]
Trait Bipolar disorder
Title Genome-wide association study of bipolar I disorder in the Han Chinese population
Risk Allele T
P-val 0.00001
Odds Ratio 1.33 [1.17-1.51]