{{Rsnum
|rsid=3024718
|Gene=PROZ
|Chromosome=13
|position=113159539
|Orientation=plus
|GMAF=0.1942
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PROZ
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 74.3 | 21.2 | 4.4
| HCB | 46.7 | 43.1 | 10.2
| JPT | 64.6 | 33.6 | 1.8
| YRI | 83.0 | 16.3 | 0.7
| ASW | 75.0 | 23.2 | 1.8
| CHB | 46.7 | 43.1 | 10.2
| CHD | 42.2 | 51.4 | 6.4
| GIH | 29.7 | 52.5 | 17.8
| LWK | 77.3 | 21.8 | 0.9
| MEX | 50.0 | 44.8 | 5.2
| MKK | 81.4 | 17.9 | 0.6
| TSI | 65.7 | 31.4 | 2.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=19050305
|Title=Association of the protein Z ATG haplotype with symptomatic nonvascular stroke or thromboembolism in white children: a family-based cohort study
}}

{{PMID Auto
|PMID=22576309
|Title=Protein Z polymorphisms associated with vaso-occlusive crisis in young sickle cell disease patients.
}}

{{PMID Auto
|PMID=23420821
|Title=Protein Z variants associated with protein Z plasma levels and with risk of idiopathic recurrent miscarriage.
}}

{{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}}