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rs12098973

From SNPedia

Orientationplus
Stabilizedplus
Make rs12098973(A;A)
Make rs12098973(A;G)
Make rs12098973(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position131937277
GeneNTM
is asnp
is mentioned by
dbSNPrs12098973
ebirs12098973
HLIrs12098973
Exacrs12098973
Varsomers12098973
Maprs12098973
PheGenIrs12098973
hapmaprs12098973
1000 genomesrs12098973
hgdprs12098973
ensemblrs12098973
gopubmedrs12098973
geneviewrs12098973
scholarrs12098973
googlers12098973
pharmgkbrs12098973
gwascentralrs12098973
openSNPrs12098973
23andMers12098973
23andMe allrs12098973
SNP Nexus

SNPshotrs12098973
SNPdbers12098973
MSV3drs12098973
GWAS Ctlgrs12098973
GMAF0.3209
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23247143OA-icon.png]
Trait Cardiac Troponin-T levels
Title Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European americans and blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.
Risk Allele G
P-val 1E-6
Odds Ratio 2.17 [1.59-3.03]