{{Rsnum
|rsid=380904
|Gene=ZC3H3
|Chromosome=8
|position=143483735
|Orientation=minus
|GMAF=0.2649
|Gene_s=ZC3H3
|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 | 54.1 | 33.3 | 12.6
| HCB | 60.3 | 33.8 | 5.9
| JPT | 49.1 | 43.6 | 7.3
| YRI | 49.7 | 40.7 | 9.7
| ASW | 46.4 | 44.6 | 8.9
| CHB | 60.3 | 33.8 | 5.9
| CHD | 52.8 | 43.4 | 3.8
| GIH | 69.3 | 27.7 | 3.0
| LWK | 46.3 | 43.5 | 10.2
| MEX | 59.6 | 38.6 | 1.8
| MKK | 37.9 | 49.0 | 13.1
| TSI | 54.0 | 43.0 | 3.0
| 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=5E-10
  |OR=1.67
  |ORtxt=[NR]
  |OA=1
}}

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