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rs12200560

From SNPedia

Orientationplus
Stabilizedplus
Make rs12200560(A;A)
Make rs12200560(A;G)
Make rs12200560(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position96632322
is asnp
is mentioned by
dbSNPrs12200560
ebirs12200560
HLIrs12200560
Exacrs12200560
Varsomers12200560
Maprs12200560
PheGenIrs12200560
hapmaprs12200560
1000 genomesrs12200560
hgdprs12200560
ensemblrs12200560
gopubmedrs12200560
geneviewrs12200560
scholarrs12200560
googlers12200560
pharmgkbrs12200560
gwascentralrs12200560
openSNPrs12200560
23andMers12200560
23andMe allrs12200560
SNP Nexus

SNPshotrs12200560
SNPdbers12200560
MSV3drs12200560
GWAS Ctlgrs12200560
GMAF0.3003
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22319020OA-icon.png]
Trait
Title A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.
Risk Allele
P-val 6E-7
Odds Ratio 1.1100 None