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)