Cardiovascular Genetic tests in Dubai & UAE

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

Tests in this category

Listed price range

2,800.00 AED

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Cardiovascular Genetic test prices

Showing 1–7 of 7 matching tests.

Cardiovascular Genetic diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4386 CACNB2 Gene Brugada Syndrome Type 4 Genetic Test This test identifies mutations in the CACNB2 gene associated with Brugada syndrome type 4, a condition predisposing to sudden cardiac arrest.	Whole Blood (Peripheral)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CACNB2 gene variants", "Pathogenic mutations"] Parameters [] Preparation [] Indications ["Diagnosis of Brugada syndrome type 4", "Risk stratification for sudden cardiac death", "Cascade family screening"] Measurement technique Confirm with laboratory Codes LOINC: 48807-7 ICD-10: I49.8 Clinical summary This test identifies mutations in the CACNB2 gene associated with Brugada syndrome type 4, a condition predisposing to sudden cardiac arrest.
TEST-4230 KCNE1 Gene (Jervell and Lange‑Nielsen Syndrome Type 2) Next‑Generation Sequencing DNA Test This test evaluates the KCNE1 gene for pathogenic variants associated with Jervell and Lange‑Nielsen syndrome type 2, a condition causing deafness and cardiac arrhythmias.	Whole Blood (EDTA), Extracted DNA, or FTA Card (DBS)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the KCNE1 gene", "Coding region analysis"] Parameters [] Preparation ["No specific fasting required.", "Provide detailed personal and family medical history.", "Genetic counselling prior to testing is highly recommended."] Indications ["Clinical suspicion of long QT syndrome", "Presence of sensorineural hearing loss", "Family history of sudden cardiac death", "Unexplained syncope"] Measurement technique Confirm with laboratory Codes LOINC: 90215-7 ICD-10: I45.81 Clinical summary This test evaluates the KCNE1 gene for pathogenic variants associated with Jervell and Lange‑Nielsen syndrome type 2, a condition causing deafness and cardiac arrhythmias.
TEST-4203 KCNE2 Gene Long QT Syndrome Type 6 Genetic Test This test identifies pathogenic variants in the KCNE2 gene, which are associated with Long QT syndrome type 6, a cardiac channelopathy.	Peripheral whole blood, extracted DNA, or dried blood spot (FTA card)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in KCNE2 gene coding exons", "Pathogenic variants in KCNE2 gene splice junctions", "Pathogenic variants in known deep intronic regions of KCNE2 gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Diagnosis of Long QT syndrome type 6", "Family cascade screening for KCNE2-related Long QT syndrome", "Guiding prophylactic beta-blocker therapy", "Informing lifestyle modifications"] Measurement technique Confirm with laboratory Codes LOINC: 91806-5 ICD-10: I45.81 Clinical summary This test identifies pathogenic variants in the KCNE2 gene, which are associated with Long QT syndrome type 6, a cardiac channelopathy.
TEST-4248 MMP3 Gene Coronary Heart Disease Susceptibility Type 6 Genetic Test This genetic test evaluates the MMP3 gene for pathogenic variants associated with inherited susceptibility to coronary heart disease type 6.	Whole Blood (3–5 mL in EDTA tube), Extracted DNA, or FTA Card Blood Spot	21–28 working days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MMP3 gene"] Parameters [] Preparation ["No fasting required", "Provide detailed family history of heart disease"] Indications ["Individuals with a family history of early-onset coronary artery disease", "Personal history suggesting increased cardiovascular risk"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Z15.09 Clinical summary This genetic test evaluates the MMP3 gene for pathogenic variants associated with inherited susceptibility to coronary heart disease type 6.
TEST-4298 PSEN2 Gene Cardiomyopathy, Dilated Type 1V Genetic Test This test evaluates the PSEN2 gene for pathogenic variants associated with dilated cardiomyopathy type 1V.	Whole Blood, Extracted DNA, or dried blood spot on FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PSEN2 gene"] Parameters [] Preparation [] Indications ["Diagnosis of suspected dilated cardiomyopathy type 1V", "Family screening for PSEN2-related cardiomyopathy", "Risk assessment in individuals with family history"] Measurement technique Confirm with laboratory Codes LOINC: 81304-2 ICD-10: I42.0 Clinical summary This test evaluates the PSEN2 gene for pathogenic variants associated with dilated cardiomyopathy type 1V.
TEST-3990 TGFB2 Gene Loeys-Dietz Syndrome Type 4 Genetic Test This test identifies pathogenic variants in the TGFB2 gene associated with Loeys-Dietz syndrome type 4, an inherited connective tissue disorder.	Whole Blood (EDTA), Extracted DNA, FTA Card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TGFB2 gene", "Single nucleotide variants", "Insertions", "Deletions", "Copy number changes"] Parameters [] Preparation ["No fasting or special preparation required"] Indications ["Personal or family history of aortic root enlargement", "Early-onset arterial aneurysms", "Suspected Loeys-Dietz spectrum disorders"] Measurement technique Confirm with laboratory Codes LOINC: 44127-1 ICD-10: Q87.89 Clinical summary This test identifies pathogenic variants in the TGFB2 gene associated with Loeys-Dietz syndrome type 4, an inherited connective tissue disorder.
TEST-4126 ZFPM2 Gene Tetralogy of Fallot Genetic Test This test identifies genetic variants in the ZFPM2 gene associated with Tetralogy of Fallot.	Whole Blood, Extracted DNA, or One Drop Blood on FTA Card	21–28 Business Days (3–4 Weeks)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ZFPM2 gene", "Likely pathogenic variants in the ZFPM2 gene"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical history", "Attend genetic counselling session (ideally)"] Indications ["Confirmation of molecular diagnosis for Tetralogy of Fallot", "Assessment of recurrence risk in future pregnancies", "Guidance for treatment planning"] Measurement technique Confirm with laboratory Codes LOINC: 82332-1 ICD-10: Q21.3 Clinical summary This test identifies genetic variants in the ZFPM2 gene associated with Tetralogy of Fallot.

Category overview

Cardiovascular Genetic: overview

Protecting your heart means looking beyond standard lipid tests to uncover the precise molecular blueprint governing your cardiovascular system. Representing a critical subspecialty within our Genetics services, Cardiovascular Genetic testing evaluates your DNA for hereditary markers linked to familial hypercholesterolemia, aortopathies, and complex vascular conditions. Utilizing cutting-edge diagnostic technology, this vital preventative screening helps identify hidden structural and metabolic risks, offering the definitive data necessary to safely guide personalized cardiology care, proactive surgical planning, and targeted medical management. Recognized for excellence in preventative diagnostics among top diagnostic labs in the UAE, DNA Labs guarantees strict patient confidentiality, unparalleled analytical accuracy, and incredibly prompt reporting. Prioritize your heart health—schedule your cardiovascular genetic testing in UAE, coordinate a comfortable home sample collection, or consult our specialized medical team.

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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.