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.
Prothrombin G20210A (Factor II) Mutation Test in New Delhi Overview
No special preparations needed
- Specimen Source
- Factor Ii (prothrombin) Mutation
This genetic test identifies mutations in the prothrombin (Factor II) gene, particularly the G20210A mutation, which increases the risk of blood clots.
It is ordered for patients with unexplained thromboembolism, family history of clotting disorders, or recurrent miscarriages.
A blood sample is collected in an EDTA tube for DNA extraction and PCR-based mutation analysis.
A positive result indicates inherited thrombophilia. Heterozygous or homozygous mutation status affects clinical risk and treatment.
No special preparation is required. Genetic counseling may be recommended for interpretation and family planning.
Test code
9893
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 3 ML |
Specimen stability information
Edta Whole Blood
Specimen rejection criteria
Test run frequency
Every Day TIME - 09:30
Turn around time
3 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
Package price
₹8100
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₹8100