Prothrombin G20210A (Factor II) Mutation
This test detects mutations in the prothrombin gene, which may increase the risk of blood clots, helping assess clotting disorders like deep vein thrombosis.
Overview of Prothrombin G20210A (Factor II) Mutation in Pathanamthitta
What is the Factor II Mutation test?
This genetic test identifies mutations in the prothrombin (Factor II) gene, particularly the G20210A mutation, which increases the risk of blood clots.
Why is the test performed?
It is ordered for patients with unexplained thromboembolism, family history of clotting disorders, or recurrent miscarriages.
What sample is needed, and how is it collected?
A blood sample is collected in an EDTA tube for DNA extraction and PCR-based mutation analysis.
How are the results interpreted?
A positive result indicates inherited thrombophilia. Heterozygous or homozygous mutation status affects clinical risk and treatment.
Is any special preparation needed before the test?
No special preparation is required. Genetic counseling may be recommended for interpretation and family planning.
Test included
- Specimen Source
- Factor Ii (prothrombin) Mutation
Doctor information
Test code
9893
CPT and Loinc codes
Department
- Advanced Molecular Diagnostics R&d
Turn around time
3 Working Days
Test run frequency
Every Day TIME - 09:30
Performing locations
3 labs across India
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 3 ML |
Specimen stability information
Edta Whole Blood
Test price
₹8595
Need Help?
Talk to our health experts for guidance on tests, reports, or bookings.
WhatsApp to Book TestProthrombin G20210A (Factor II) Mutation
₹8595