{{Rsnum
|rsid=12098973
|Gene=NTM
|Chromosome=11
|position=131937277
|Orientation=plus
|GMAF=0.3209
|Gene_s=NTM
|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 | 70.5 | 25.9 | 3.6
| HCB | 54.0 | 38.0 | 8.0
| JPT | 47.8 | 42.5 | 9.7
| YRI | 5.4 | 33.3 | 61.2
| ASW | 17.5 | 38.6 | 43.9
| CHB | 54.0 | 38.0 | 8.0
| CHD | 61.5 | 33.9 | 4.6
| GIH | 42.6 | 41.6 | 15.8
| LWK | 18.2 | 36.4 | 45.5
| MEX | 77.6 | 20.7 | 1.7
| MKK | 20.5 | 43.6 | 35.9
| TSI | 68.6 | 26.5 | 4.9
| 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=G
  |Pval=1E-6
  |OR=2.17
  |ORtxt=[1.59-3.03]
  |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 | Illumina Human 1M}}