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rs1526687

From SNPedia

Orientationplus
Stabilizedplus
Make rs1526687(G;G)
Make rs1526687(G;T)
Make rs1526687(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position52486669
is asnp
is mentioned by
dbSNPrs1526687
ebirs1526687
HLIrs1526687
Exacrs1526687
Varsomers1526687
Maprs1526687
PheGenIrs1526687
hapmaprs1526687
1000 genomesrs1526687
hgdprs1526687
ensemblrs1526687
gopubmedrs1526687
geneviewrs1526687
scholarrs1526687
googlers1526687
pharmgkbrs1526687
gwascentralrs1526687
openSNPrs1526687
23andMers1526687
23andMe allrs1526687
SNP Nexus

SNPshotrs1526687
SNPdbers1526687
MSV3drs1526687
GWAS Ctlgrs1526687
GMAF0.1414
Max Magnitude
? (G;G) (G;T) (T;T) 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 T
P-val 5E-6
Odds Ratio .04 [0.02-0.06] ug/L increase