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rs12725198

From SNPedia

Orientationplus
Stabilizedplus
Make rs12725198(A;A)
Make rs12725198(A;G)
Make rs12725198(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position15753676
is asnp
is mentioned by
dbSNPrs12725198
ebirs12725198
HLIrs12725198
Exacrs12725198
Varsomers12725198
Maprs12725198
PheGenIrs12725198
hapmaprs12725198
1000 genomesrs12725198
hgdprs12725198
ensemblrs12725198
gopubmedrs12725198
geneviewrs12725198
scholarrs12725198
googlers12725198
pharmgkbrs12725198
gwascentralrs12725198
openSNPrs12725198
23andMers12725198
23andMe allrs12725198
SNP Nexus

SNPshotrs12725198
SNPdbers12725198
MSV3drs12725198
GWAS Ctlgrs12725198
GMAF0.1694
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 A
P-val 3E-6
Odds Ratio 1.85 [1.43-2.39]