{{Rsnum
|rsid=12564445
|Gene=TNNT2
|Chromosome=1
|position=201376359
|Orientation=plus
|GMAF=0.2746
|Gene_s=TNNT2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.8 | 25.9 | 72.3
| HCB | 13.2 | 42.6 | 44.1
| JPT | 3.5 | 52.2 | 44.2
| YRI | 16.3 | 52.4 | 31.3
| ASW | 15.8 | 49.1 | 35.1
| CHB | 13.2 | 42.6 | 44.1
| CHD | 4.7 | 49.1 | 46.2
| GIH | 8.0 | 34.0 | 58.0
| LWK | 23.6 | 44.5 | 31.8
| MEX | 0.0 | 37.9 | 62.1
| MKK | 23.1 | 55.8 | 21.2
| TSI | 1.0 | 29.4 | 69.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23247143
  |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.
  |RiskAllele=A
  |Pval=5E-8
  |OR=2.33
  |ORtxt=[1.72-3.16]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}