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rs2123536

From SNPedia

Orientationminus
Stabilizedminus
Make rs2123536(A;A)
Make rs2123536(A;G)
Make rs2123536(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position19745816
is asnp
is mentioned by
dbSNPrs2123536
ebirs2123536
HLIrs2123536
Exacrs2123536
Varsomers2123536
Maprs2123536
PheGenIrs2123536
hapmaprs2123536
1000 genomesrs2123536
hgdprs2123536
ensemblrs2123536
gopubmedrs2123536
geneviewrs2123536
scholarrs2123536
googlers2123536
pharmgkbrs2123536
gwascentralrs2123536
openSNPrs2123536
23andMers2123536
23andMe allrs2123536
SNP Nexus

SNPshotrs2123536
SNPdbers2123536
MSV3drs2123536
GWAS Ctlgrs2123536
GMAF0.2268
Max Magnitude
? (A;A) (A;G) (G;G) 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 7E-11
Odds Ratio 1.12 [1.08-1.16]