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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.