{{Rsnum
|rsid=13083990
|Chromosome=3
|position=122295719
|Orientation=plus
|GMAF=0.3453
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 46.0 | 46.0
| HCB | 29.2 | 49.6 | 21.2
| JPT | 28.3 | 53.1 | 18.6
| YRI | 2.0 | 13.6 | 84.4
| ASW | 0.0 | 14.0 | 86.0
| CHB | 29.2 | 49.6 | 21.2
| CHD | 32.1 | 41.3 | 26.6
| GIH | 37.6 | 44.6 | 17.8
| LWK | 0.0 | 15.5 | 84.5
| MEX | 13.8 | 50.0 | 36.2
| MKK | 1.3 | 25.6 | 73.1
| TSI | 19.6 | 49.0 | 31.4
| 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=T
  |Pval=4E-6
  |OR=2.66
  |ORtxt=[1.76-4.02]
  |OA=1
}}

{{PMID Auto
|PMID=23125333
|Title=Common genetic variation of the calcium-sensing receptor and lethal prostate cancer risk.
|OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}