Thrombophilia Panel tests in Dubai & UAE

Compare available Thrombophilia Panel tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

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Listed price range

1,500.00–3,500.00 AED

Clinical preparation

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Thrombophilia Panel test prices

Showing 1–4 of 4 matching tests.

Thrombophilia Panel diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1378 Thrombophilia Genetic Panel (MTHFR, Factor V Leiden, Prothrombin G20210A) Test This genetic panel evaluates for three specific inherited mutations associated with an increased risk of blood clot formation.	Peripheral whole blood	3–4 days	1,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MTHFR C677T gene mutation", "Factor V Leiden (G1691A) gene mutation", "Prothrombin G20210A gene mutation"] Parameters [{"name": "MTHFR C677T", "reference_range": "Homozygous Wild-Type (CC), Heterozygous (CT), Homozygous Mutant (TT)"}, {"name": "Factor V Leiden (G1691A)", "reference_range": "Homozygous Wild-Type (GG), Heterozygous (GA), Homozygous Mutant (AA)"}, {"name": "Prothrombin G20210A", "reference_range": "Homozygous Wild-Type (GG), Heterozygous (GA), Homozygous Mutant (AA)"}] Preparation ["No fasting required", "Hydrate well", "Bring doctor's prescription or valid ID for home collection"] Indications ["Personal or family history of venous thromboembolism", "Evaluation before major surgery", "Investigation of recurrent pregnancy loss", "Assessment of risk in specific medical conditions"] Measurement technique Confirm with laboratory Codes LOINC: 24331-0 ICD-10: Z13.79 Clinical summary This genetic panel evaluates for three specific inherited mutations associated with an increased risk of blood clot formation.
TEST-3276 Thrombophilia Profile Test This diagnostic test evaluates genetic mutations and functional protein levels associated with an increased risk of blood clot formation.	Peripheral whole blood (sodium citrate, EDTA) and serum	3–4 working days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Factor V Leiden mutation", "Prothrombin G20210A mutation", "MTHFR C677T/A1298C mutations", "Protein C levels", "Protein S levels", "Antithrombin III levels", "Lupus Anticoagulant", "Anticardiolipin antibodies", "Anti-β2 Glycoprotein I antibodies"] Parameters [{"name": "Factor V Leiden", "reference_range": "Negative/Positive"}, {"name": "Prothrombin G20210A", "reference_range": "Negative/Positive"}, {"name": "MTHFR C677T", "reference_range": "Homozygous/Heterozygous/Wild-type"}, {"name": "MTHFR A1298C", "reference_range": "Homozygous/Heterozygous/Wild-type"}, {"name": "Protein C", "reference_range": "70-140%"}, {"name": "Protein S", "reference_range": "60-150%"}, {"name": "Antithrombin III", "reference_range": "80-120%"}, {"name": "Lupus Anticoagulant", "reference_range": "Negative/Positive"}, {"name": "Anticardiolipin IgG", "reference_range": " Preparation ["Overnight fasting is preferred.", "Discontinue heparin 1 day prior.", "Discontinue oral anticoagulants (warfarin, DOACs) 7 days prior, only with physician approval.", "Complete and sign the Coagulation Requisition Form (Form 15)."] Indications ["Evaluation of inherited thrombophilia", "Investigation of acquired thrombophilia (antiphospholipid syndrome)", "Risk assessment for venous thromboembolism (VTE)", "Pre-operative risk assessment in certain cases", "Evaluation of recurrent pregnancy loss"] Measurement technique Confirm with laboratory Codes LOINC: 55635-5 ICD-10: D68.59 Clinical summary This diagnostic test evaluates genetic mutations and functional protein levels associated with an increased risk of blood clot formation.
TEST-3285 Thrombophilia Total Profile Test This diagnostic test evaluates inherited genetic factors and acquired functional protein deficiencies associated with an increased risk of blood clot formation.	Whole blood (citrate, EDTA, SST)	3–5 working days	3,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Factor V Leiden", "Prothrombin G20210A", "MTHFR variants", "Protein C deficiency", "Protein S deficiency", "Antithrombin III deficiency", "Lupus anticoagulant", "Factor VIII levels"] Parameters [{"name": "Factor V Leiden", "reference_range": "Negative/Positive"}, {"name": "Prothrombin G20210A", "reference_range": "Negative/Positive"}, {"name": "MTHFR C677T", "reference_range": "Homozygous/Heterozygous/Wild-type"}, {"name": "MTHFR A1298C", "reference_range": "Homozygous/Heterozygous/Wild-type"}, {"name": "Protein C Activity", "reference_range": "70-130%"}, {"name": "Protein S Activity", "reference_range": "60-140%"}, {"name": "Antithrombin III Activity", "reference_range": "80-120%"}, {"name": "Lupus Anticoagulant", "reference_range": "Negative/Positive"}, {"name": "Factor VIII Activity", "reference_range": "50-150%"}] Preparation ["Fasting overnight (8–12 hours)", "Discontinue heparin 24 hours prior with physician approval", "Discontinue warfarin/direct oral anticoagulants 7 days prior with physician approval", "Provide a duly filled Coagulation Requisition Form (Form 15)"] Indications ["Evaluation of risk for venous thromboembolism", "Investigation of recurrent pregnancy loss", "Assessment of unexplained thrombosis", "Pre-operative risk assessment in certain cases"] Measurement technique Confirm with laboratory Codes LOINC: 34535-2 ICD-10: D68.59, Z15.01, Z86.72 Clinical summary This diagnostic test evaluates inherited genetic factors and acquired functional protein deficiencies associated with an increased risk of blood clot formation.
TEST-3371 Venous Thrombosis Risk Analysis Panel Test This genetic panel evaluates inherited mutations associated with an increased risk of venous thromboembolism.	Whole Blood	5 Working Days from Sample Receipt	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Factor V Leiden (G1691A) mutation", "Prothrombin G20210A mutation", "MTHFR C677T polymorphism", "MTHFR A1298C polymorphism"] Parameters [{"name": "Factor V Leiden (G1691A)", "reference_range": "Negative / Positive"}, {"name": "Prothrombin G20210A", "reference_range": "Negative / Positive"}, {"name": "MTHFR C677T", "reference_range": "Negative / Positive"}, {"name": "MTHFR A1298C", "reference_range": "Negative / Positive"}] Preparation ["No fasting required", "Continue all prescribed medications unless instructed otherwise by your doctor", "Maintain normal hydration"] Indications ["Assessment of inherited thrombophilia risk", "Pre-surgical risk stratification", "Evaluation in patients with unexplained VTE", "Family history of thrombophilia"] Measurement technique Confirm with laboratory Codes LOINC: 34718-2 ICD-10: Z15.09 Clinical summary This genetic panel evaluates inherited mutations associated with an increased risk of venous thromboembolism.

Category overview

Thrombophilia Panel: overview

Experiencing recurrent blood clots or unexplained pregnancy loss requires a comprehensive, overarching view of your body's coagulation system to find targeted relief. Within our advanced Hematology department, the comprehensive Thrombophilia Panel evaluates multiple genetic and acquired risk factors—such as Factor V Leiden, prothrombin mutations, and specific antibodies—that dangerously increase your risk of abnormal clotting. By leveraging state-of-the-art diagnostic technology, this expansive hemostatic screening helps uncover the precise biological drivers behind your symptoms, safely guiding personalized blood-thinning protocols and proactive maternal-fetal care. Recognized for clinical excellence among premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, uncompromising diagnostic accuracy, and remarkably fast turnaround times. Safeguard your vascular future—book your thrombophilia panel testing in UAE, arrange a secure clinical sample collection, or consult our dedicated medical specialists today.

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Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.