{{Rsnum
|rsid=2050190
|Gene=C6orf10
|Chromosome=6
|position=32371299
|Orientation=minus
|GMAF=0.3664
|Gene_s=C6orf10
|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 | 4.4 | 41.6 | 54.0
| HCB | 12.6 | 52.6 | 34.8
| JPT | 9.7 | 46.9 | 43.4
| YRI | 28.5 | 49.3 | 22.2
| ASW | 23.2 | 48.2 | 28.6
| CHB | 12.6 | 52.6 | 34.8
| CHD | 14.0 | 52.3 | 33.6
| GIH | 11.9 | 42.6 | 45.5
| LWK | 29.6 | 44.4 | 25.9
| MEX | 7.0 | 36.8 | 56.1
| MKK | 17.3 | 48.1 | 34.6
| TSI | 15.7 | 43.1 | 41.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22703881
|Trait=None
|Title=Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease.
|RiskAllele=A
|Pval=7E-7
|OR=0.2528
|ORtxt=None
|OA=1
}}

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