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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.

Also known asprothrombin g20210a mutationfactor ii mutationprothrombin gene mutationprothrombin g20210a (factor ii) mutation

Available via

Home Collection, Lab Visit

Contains

2 parameters

Earliest reports in

3 Working Days

Test details

Prothrombin G20210A (Factor II) Mutation Test in Kolkata Overview

Preparations

No special preparations needed

Test included
Prothrombin G20210A (Factor II) Mutation includes 2 parameters

  • Specimen Source
  • Factor Ii (prothrombin) Mutation
Frequently Asked Questions

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
SpecimenVacutainerVolume
Edta Whole BloodLavender Vacutainer3 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

Prothrombin G20210A (Factor II) Mutation

₹8100

Health Checkup Category

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Prothrombin G20210A (Factor II) Mutation Test in Other Cities

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