{{Rsnum
|rsid=6020
|Gene=F5
|Chromosome=1
|position=169549874
|Orientation=minus
|GMAF=0.2649
|Gene_s=F5
|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 | 1.8 | 98.2
| HCB | 39.3 | 50.4 | 10.4
| JPT | 49.1 | 40.0 | 10.9
| YRI | 7.5 | 45.9 | 46.6
| ASW | 3.5 | 35.1 | 61.4
| CHB | 39.3 | 50.4 | 10.4
| CHD | 34.9 | 49.5 | 15.6
| GIH | 1.0 | 25.7 | 73.3
| LWK | 10.1 | 45.0 | 45.0
| MEX | 0.0 | 16.4 | 83.6
| MKK | 7.1 | 32.7 | 60.3
| TSI | 0.0 | 5.9 | 94.1
| HapMapRevision=28
}}{{PMID Auto
|PMID=23954867
|Title=The association of idiopathic recurrent pregnancy loss with polymorphisms in haemostasis-related genes
}}

{{PMID Auto
|PMID=18974781
|Title=Cataloging coding sequence variations in human genome databases.
|OA=1
}}

{{PMID Auto
|PMID=25119470
|Title=Single Nucleotide Polymorphisms Other than Factor V Leiden Are Associated with Coagulopathy and Osteonecrosis of the Femoral Head in Chinese Patients
}}
{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}