Diagnostic options · UAE

Cardiogenetics tests in Dubai & UAE

Compare available Cardiogenetics 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

Clinical preparation

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Cardiogenetics test prices

Showing 1–6 of 6 matching tests.

Cardiogenetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4121 AGK Gene Genetic Test for Sengers Syndrome This test evaluates the AGK gene for pathogenic variants associated with Sengers syndrome.	Peripheral whole blood (EDTA)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single-nucleotide variants in AGK gene", "Small insertions/deletions in AGK gene", "Copy-number variations in AGK gene"] Parameters [] Preparation ["Genetic counselling session required prior to sample collection", "Inform phlebotomist if on anticoagulant therapy"] Indications ["Clinical suspicion of Sengers syndrome", "Family history of Sengers syndrome", "Cascade family screening"] Measurement technique Confirm with laboratory Codes LOINC: 21641-0 ICD-10: E88.4, E88.49 Clinical summary This test evaluates the AGK gene for pathogenic variants associated with Sengers syndrome.
TEST-4183 CALM2 Gene Long QT Syndrome Type 15 Genetic Test This test evaluates the CALM2 gene for pathogenic variants associated with Long QT syndrome type 15.	Peripheral Whole Blood or Buccal Swab (DNA 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 CALM2 gene"] Parameters [] Preparation ["Continue all prescribed medications unless instructed otherwise by your physician", "Mandatory genetic counseling session required"] Indications ["Suspected Long QT syndrome type 15", "Family history of Long QT syndrome or sudden cardiac death"] Measurement technique Confirm with laboratory Codes LOINC: 81237-0 ICD-10: I45.81 Clinical summary This test evaluates the CALM2 gene for pathogenic variants associated with Long QT syndrome type 15.
TEST-2942 FOXH1 Gene Test This test detects pathogenic variants in the FOXH1 gene associated with congenital heart disease and transposition of the great arteries.	Whole Blood (EDTA), Extracted DNA, or 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 FOXH1 gene", "Single nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation [] Indications ["Neonatal and paediatric patients with suspected congenital heart disease", "Patients with suspected transposition of the great arteries", "Family screening for CHD"] Measurement technique Confirm with laboratory Codes LOINC: 103206-3 ICD-10: Q20.3, Q24.9 Clinical summary This test detects pathogenic variants in the FOXH1 gene associated with congenital heart disease and transposition of the great arteries.
TEST-3073 GATA4 Gene Atrial Septal Defect Type 2 Genetic Test This test identifies pathogenic variants in the GATA4 gene associated with autosomal dominant atrial septal defect type 2.	Peripheral whole blood (EDTA tube) 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 ["GATA4 gene sequence", "Copy Number Variations (CNVs) in GATA4"] Parameters [] Preparation ["No specific fasting required.", "Do not discontinue cardiac medications without consulting a physician."] Indications ["Diagnosis of ASD Type 2", "Family cascade screening for ASD Type 2", "Risk stratification for individuals with family history"] Measurement technique Confirm with laboratory Codes LOINC: 82533-6 ICD-10: Q21.1, Z15.09, Z13.6 Clinical summary This test identifies pathogenic variants in the GATA4 gene associated with autosomal dominant atrial septal defect type 2.
TEST-4408 TBX20 Gene Atrial Septal Defect Type 4 Genetic Test This test evaluates the TBX20 gene for mutations associated with Atrial Septal Defect Type 4 (ASD4). It uses Next Generation Sequencing (NGS) to detect pathogenic variants.	Peripheral Whole Blood	3–4 Weeks (21–28 Business Days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic single-nucleotide variants in TBX20", "Insertions and deletions in TBX20 coding region", "Splice-site boundaries of TBX20"] Parameters [] Preparation ["No specific fasting required.", "Inform physician about known interfering medications."] Indications ["Diagnosis of Atrial Septal Defect Type 4 (ASD4)", "Family cascade screening for TBX20-related ASD4", "Guiding clinical management decisions for ASD4"] Measurement technique Confirm with laboratory Codes LOINC: 48018-6 ICD-10: Q21.1 Clinical summary This test evaluates the TBX20 gene for mutations associated with Atrial Septal Defect Type 4 (ASD4). It uses Next Generation Sequencing (NGS) to detect pathogenic variants.
TEST-4403 TLL1 Gene Atrial Septal Defect Type 6 Genetic Test This test identifies pathogenic variants in the TLL1 gene associated with atrial septal defect type 6 (ASD6).	Peripheral blood (whole blood, EDTA tube)	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 TLL1 gene", "Single nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["No fasting required"] Indications ["Clinical suspicion of atrial septal defect type 6 (ASD6)", "Congenital heart malformation"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q21.1 Clinical summary This test identifies pathogenic variants in the TLL1 gene associated with atrial septal defect type 6 (ASD6).

Category overview

Cardiogenetics: overview

A strong family history of sudden heart issues demands precise answers, providing you with the ultimate foundation for proactive, preventive cardiovascular care. As part of our Molecular Diagnostics division, our advanced Cardiogenetics testing utilizes high-throughput next-generation sequencing to deeply analyze a wide array of genetic markers associated with inherited heart conditions. Rather than making a definitive standalone diagnosis, this expansive cardiogenetics data empowers your cardiology team with the critical molecular clarity required for highly customized, preventive medical guidance. Renowned among leading diagnostic labs in Dubai and the UAE, DNA Labs UAE ensures strict patient confidentiality and exceptionally fast, highly accurate turnaround times. Take control of your long-term heart health: discover our cardiogenetics testing in the UAE below to book your test, arrange a seamless home collection, or consult our medical professionals.

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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.