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0056200
Thrombotic Risk, DNA Panel
THROMDNA
Ordering Recommendation
Acceptable panel to detect the two most common inherited thrombophilias: factor V Leiden related (R506Q variant of the F5 gene) and prothrombin related (G20210A variant of the F2 gene). This panel also detects thrombophilia associated with pathogenic variants in the MTHFR gene (c.665C>T and c.1286A>C).
New York DOH Approval Status
This test is New York state approved.
Specimen Required
Patient Preparation
Collect
Lavender (EDTA), pink (K2EDTA) or yellow (ACD solution A or B).
Specimen Preparation
Transport 4 mL whole blood. (Min: 3 mL)
Storage/Transport Temperature
Refrigerated.
Unacceptable Conditions
Plasma or serum; collection of specimen in sodium heparin tubes. Frozen specimens in glass collection tubes.
Remarks
Stability
Ambient: 72 hours; Refrigerated: 1 week; Frozen: 1 month.
Methodology
Polymerase Chain Reaction (PCR)
Fluorescence Monitoring
Performed
Sun-Sat
Reported
2-6 days
Reference Interval
Interpretive Data
Refer to report
Compliance Category
Laboratory Developed Test (LDT)
Note
Hotline History
N/A
CPT Codes
81240; 81241; 81291
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
- FVL R506Q, MTHFR, and Factor II mutation panel
- Hypercoag
- Hypercoagulable Panel
Thrombotic Risk, DNA Panel
