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rs886126

From SNPedia

Orientationplus
Stabilizedplus
Make rs886126(C;C)
Make rs886126(C;T)
Make rs886126(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position111241410
GeneCUX2
is asnp
is mentioned by
dbSNPrs886126
ebirs886126
HLIrs886126
Exacrs886126
Varsomers886126
Maprs886126
PheGenIrs886126
hapmaprs886126
1000 genomesrs886126
hgdprs886126
ensemblrs886126
gopubmedrs886126
geneviewrs886126
scholarrs886126
googlers886126
pharmgkbrs886126
gwascentralrs886126
openSNPrs886126
23andMers886126
23andMe allrs886126
SNP Nexus

SNPshotrs886126
SNPdbers886126
MSV3drs886126
GWAS Ctlgrs886126
GMAF0.4463
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23364394]
Trait Coronary heart disease
Title A genome-wide association study of a coronary artery disease risk variant.
Risk Allele T
P-val 1E-6
Odds Ratio 1.14 [1.08-1.20]