{{Rsnum
|rsid=6028
|Gene=F5
|Chromosome=1
|position=169582444
|Orientation=plus
|GMAF=0.2282
|Gene_s=F5
|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 | 7.7 | 46.2 | 46.2
| HCB | 4.4 | 33.3 | 62.2
| JPT | 6.8 | 45.5 | 47.7
| YRI | 0.0 | 3.2 | 96.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 4.4 | 33.3 | 62.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22703881
|Trait=None
|Title=Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease.
|RiskAllele=C
|Pval=3E-9
|OR=0.2260
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=18426996
|Title=Relations of inflammatory biomarkers and common genetic variants with arterial stiffness and wave reflection.
|OA=1
}}

{{PMID Auto
|PMID=19404301
|Title=Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}