{{Rsnum
|rsid=12725198
|Chromosome=1
|position=15753676
|Orientation=plus
|GMAF=0.1694
|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 | 7.1 | 31.2 | 61.6
| HCB | 2.2 | 10.9 | 86.9
| JPT | 0.0 | 12.4 | 87.6
| YRI | 2.7 | 40.8 | 56.5
| ASW | 3.5 | 31.6 | 64.9
| CHB | 2.2 | 10.9 | 86.9
| CHD | 0.0 | 22.0 | 78.0
| GIH | 2.0 | 35.6 | 62.4
| LWK | 1.8 | 24.5 | 73.6
| MEX | 0.0 | 44.8 | 55.2
| MKK | 12.2 | 39.1 | 48.7
| TSI | 8.8 | 35.3 | 55.9
| 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=3E-6
  |OR=1.85
  |ORtxt=[1.43-2.39]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}