Hereditary Thrombophilia Panel
The two variants most frequently tested in an inherited clotting-risk workup: Factor V Leiden and the prothrombin G20210A variant.
2 genes · 2 variants
F5gene ↗
coagulation factor V
F5 is a human protein-coding gene.
F2gene ↗
coagulation factor II, thrombin
F2 is a human protein-coding gene.
rs6025variant ↗
F5 · p.Arg534Gln
rs6025 is a genetic variant located in the F5 gene.
rs1799963variant ↗
F2
rs1799963 is a genetic variant located in the F2 gene.
Educational information only — not medical advice, a diagnosis, or a clinical recommendation. This panel is a curated grouping of public-record gene and variant pages for reference; it does not reflect your own genome or personal risk. Consult a qualified genetics professional or genetic counselor for interpretation relevant to you.