{{Rsnum
|rsid=10504130
|Gene=PCMTD1
|Chromosome=8
|position=51844533
|Orientation=plus
|GMAF=0.1299
|Gene_s=PCMTD1
|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 | 0.0 | 21.2 | 78.8
| HCB | 1.5 | 28.5 | 70.1
| JPT | 1.8 | 36.3 | 61.9
| YRI | 0.0 | 2.7 | 97.3
| ASW | 0.0 | 15.8 | 84.2
| CHB | 1.5 | 28.5 | 70.1
| CHD | 0.9 | 28.4 | 70.6
| GIH | 2.0 | 25.7 | 72.3
| LWK | 0.0 | 7.3 | 92.7
| MEX | 3.4 | 13.8 | 82.8
| MKK | 0.6 | 14.7 | 84.6
| TSI | 2.0 | 23.5 | 74.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=G
  |Pval=4E-9
  |OR=1.88
  |ORtxt=[NR]
  |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}}