{{Rsnum
|rsid=7714670
|Gene=CCDC39
|Chromosome=5
|position=73776529
|Orientation=plus
|GMAF=0.377
|Gene_s=CCDC39
|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 | 16.8 | 55.8 | 27.4
| HCB | 8.0 | 43.8 | 48.2
| JPT | 8.8 | 43.4 | 47.8
| YRI | 10.2 | 42.2 | 47.6
| ASW | 12.3 | 54.4 | 33.3
| CHB | 8.0 | 43.8 | 48.2
| CHD | 7.4 | 38.9 | 53.7
| GIH | 12.0 | 56.0 | 32.0
| LWK | 9.1 | 39.1 | 51.8
| MEX | 12.1 | 48.3 | 39.7
| MKK | 12.8 | 49.4 | 37.8
| TSI | 21.6 | 50.0 | 28.4
| 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=A
  |Pval=2E-9
  |OR=1.52
  |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 | FTDNA}}
{{on chip | Illumina Human 1M}}