{{Rsnum
|rsid=1198872
|Gene=ATP6V1C2
|Chromosome=2
|position=10763286
|Orientation=plus
|GMAF=0.4284
|Gene_s=ATP6V1C2
|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 | 38.1 | 51.3 | 10.6
| HCB | 24.8 | 54.7 | 20.4
| JPT | 17.9 | 54.5 | 27.7
| YRI | 38.4 | 45.9 | 15.8
| ASW | 24.6 | 50.9 | 24.6
| CHB | 24.8 | 54.7 | 20.4
| CHD | 29.4 | 51.4 | 19.3
| GIH | 46.5 | 36.6 | 16.8
| LWK | 32.7 | 50.9 | 16.4
| MEX | 38.6 | 42.1 | 19.3
| MKK | 32.1 | 45.5 | 22.4
| TSI | 38.2 | 51.0 | 10.8
| 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=2E-6
  |OR=2.04
  |ORtxt=[1.51-2.74]
  |OA=1
}}

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