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rs1842896

From SNPedia

Orientationplus
Stabilizedplus
Make rs1842896(G;G)
Make rs1842896(G;T)
Make rs1842896(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position155590307
is asnp
is mentioned by
dbSNPrs1842896
ebirs1842896
HLIrs1842896
Exacrs1842896
Varsomers1842896
Maprs1842896
PheGenIrs1842896
hapmaprs1842896
1000 genomesrs1842896
hgdprs1842896
ensemblrs1842896
gopubmedrs1842896
geneviewrs1842896
scholarrs1842896
googlers1842896
pharmgkbrs1842896
gwascentralrs1842896
openSNPrs1842896
23andMers1842896
23andMe allrs1842896
SNP Nexus

SNPshotrs1842896
SNPdbers1842896
MSV3drs1842896
GWAS Ctlgrs1842896
GMAF0.449
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22751097OA-icon.png]
Trait Coronary heart disease
Title Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Risk Allele T
P-val 1E-11
Odds Ratio 1.14 [1.10-1.19]