Cardiovascular Risk Panel

12 Mutations

Our Cardiovascular Risk Panel provides comprehensive genetic testing to assess inherited thrombophilic factors and other genetic risks related to cardiovascular diseases.

This panel includes the analysis of 12 key genetic mutations:

  • Factor II Prothrombin (G20210A)
  • Factor V (G1691A, H1299R)
  • MTHFR (C677T, A1298C)
  • Factor XIII (V34L)
  • β-Fibrinogen (-455 G-A)
  • PAI-1 (4G/5G)
  • HPA-1 (a/b)
  • ACE (I/D)
  • ApoB (R3500Q)
  • ApoE (e2/e3/e4)

"The discovery of the structure of DNA transformed not only biology but also our understanding of what it means to be human."

Francis Crick