{{Rsnum
|rsid=10516089
|Gene=C5orf50
|Chromosome=5
|position=171724227
|Orientation=plus
|GMAF=0.3646
|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 | 46.0 | 49.6
| HCB | 16.2 | 44.9 | 39.0
| JPT | 11.5 | 51.3 | 37.2
| YRI | 20.4 | 49.7 | 29.9
| ASW | 3.5 | 40.4 | 56.1
| CHB | 16.2 | 44.9 | 39.0
| CHD | 12.8 | 49.5 | 37.6
| GIH | 1.0 | 36.6 | 62.4
| LWK | 17.3 | 42.7 | 40.0
| MEX | 17.2 | 37.9 | 44.8
| MKK | 9.6 | 39.7 | 50.6
| TSI | 11.8 | 42.2 | 46.1
| 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=
  |Pval=4E-9
  |OR=1.59
  |ORtxt=[NR]
  |OA=1
}}

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