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rs2660899

From SNPedia

Orientationplus
Stabilizedplus
Make rs2660899(G;G)
Make rs2660899(G;T)
Make rs2660899(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position96036642
GeneLTA4H
is asnp
is mentioned by
dbSNPrs2660899
ebirs2660899
HLIrs2660899
Exacrs2660899
Varsomers2660899
Maprs2660899
PheGenIrs2660899
hapmaprs2660899
1000 genomesrs2660899
hgdprs2660899
ensemblrs2660899
gopubmedrs2660899
geneviewrs2660899
scholarrs2660899
googlers2660899
pharmgkbrs2660899
gwascentralrs2660899
openSNPrs2660899
23andMers2660899
23andMe allrs2660899
SNP Nexus

SNPshotrs2660899
SNPdbers2660899
MSV3drs2660899
GWAS Ctlgrs2660899
GMAF0.2691
Max Magnitude
? (G;G) (G;T) (T;T) 28
Despite earlier reports of an association, no risk for myocardial infarction was seen for rs2660899 variants in a study of 1,211 German patients. [PMID 18318662]