Thrombophilia

Last Updated Feb 4, 2022

Genetic screening of variants associated with thrombosis. Common variants associated with thrombosis are Factor V Leiden, Prothrombin 20210 G>A, Methylenetetrahydrofolate reductase (MTHFR) C677T variants. They are usually screened by PCR and RFLP or by sequencing. 

Inherited thrombophilia is a genetic predisposition to developing thromboembolic complications. These prothrombotic risk factors include defects of coagulation factor inhibitors, increased levels or function of coagulation factors, fibrinolytic system, platelet function, and hyperhomocysteinemia. Common variants associated with thrombosis are Factor V Leiden, Prothrombin 20210 G>A, Methylenetetrahydrofolate reductase (MTHFR) C677T variants. They are usually screened by PCR and restriction fragment length polymorphism (RFLP) or by sequencing.

Note : The above methodology describes the approach to diagnosis followed in CMC, Vellore. This is not a recommendation or guidelines, participants are free to choose their own methodology(ies).

Participation Fee : 1500 INR

Participation Fee - As package

If you choose to participate in assessments by choosing them as a package, here is the pricing. You can choose any ONE package and can choose any other assessment individually that does not include in your chosen package.

Package 1 - Benign Molecular Haematology

12,500 INR Per EQAS

  • Haemophilia A
  • Haemophilia B
  • Beta Thalassemia
  • Alpha Thalassemia
  • Thrombophilia

Package 2 - Malignant Molecular Haematology

9,500 INR Per EQAS

  • JAK2 V617F
  • NPM1/FLT3 ANALYSIS
  • RT PCR BCR-ABL1/PML-RARA
  • FISH for t(9;22)(q34;q11) BCR::ABL1

Package 3
All the tests

21,500 INR Per EQAS

  • Haemophilia A
  • Haemophilia B
  • Beta Thalassemia
  • Alpha Thalassemia
  • Thrombophilia
  • JAK2 V617F
  • NPM1/FLT3 ANALYSIS
  • RT PCR BCR-ABL1/PML-RARA
  • FISH for t(9;22)(q34;q11) BCR::ABL1
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