{{Rsnum
|rsid=4524
|Gene=F5
|Chromosome=1
|position=169542517
|Orientation=minus
|GMAF=0.2438
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=F5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 54.9 | 38.1 | 7.1
| HCB | 66.4 | 32.1 | 1.5
| JPT | 62.8 | 33.6 | 3.5
| YRI | 68.7 | 29.3 | 2.0
| ASW | 52.6 | 40.4 | 7.0
| CHB | 66.4 | 32.1 | 1.5
| CHD | 59.6 | 35.8 | 4.6
| GIH | 36.6 | 56.4 | 6.9
| LWK | 66.4 | 31.8 | 1.8
| MEX | 41.4 | 34.5 | 24.1
| MKK | 53.2 | 41.7 | 5.1
| TSI | 57.8 | 36.3 | 5.9
| HapMapRevision=28
}}Gene variants associated with [[deep vein thrombosis]].{{PMID|18349091}}

Updated analysis of gene variants associated with [[deep vein thrombosis]].{{PMID|20124536}}

{{PMID Auto
|PMID=20031567
|Title=An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=22533697
|Title=Candidate gene polymorphisms and the risk for pregnancy-related venous thrombosis.
}}

{{GET Evidence
|gene=F5
|aa_change=Lys858Arg
|aa_change_short=K858R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4524
|overall_frequency_n=2624
|overall_frequency_d=10758
|overall_frequency=0.243912
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=28
|n_articles=0
|n_articles_annotated=0
|qualityscore_in_silico=3
|qualitycomment_in_silico=Y
|gene_in_genetests=Y
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=-3
|autoscore=3
|n_web_uneval=5
}}

{{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}}