Acceptable panel to detect the two most common inherited thrombophilias (prothrombin related and factor V Leiden related).
Polymerase Chain Reaction/Fluorescence Monitoring
Lavender (EDTA), pink (K2 EDTA) or yellow (ACD Solution A or B).
Transport 3 mL whole blood. (Min: 2 mL)
Plasma or serum; collection of specimen in sodium heparin tubes.
Ambient: 72 hours; Refrigerated: 1 week; Frozen: 1 month.
|0097720||Factor V Leiden (F5) R506Q Mutation||Negative: This sample is negative for factor V Leiden, R506Q mutation.|
|0055655||Methylenetetrahydrofolate Reductase (MTHFR) 2 Variants||Negative: Neither of the MTHFR variants tested, c.665C>T (previously designated C677T) and c.1286A>C (previously designated A1298C), were detected. Other causes of elevated homocysteine levels were not evaluated.|
|0056060||Prothrombin (F2) c.*97G>A (G20210A) Pathogenic Variant|
Refer to report
No compliance statements are in use for this test.
81240; 81241; 81291
|Component Test Code*||Component Chart Name||LOINC|
- FVL R506Q, MTHFR, and Factor II mutation panel
- Hypercoagulable Panel