Cardiac Genetics tests in Dubai & UAE

Compare available Cardiac Genetics 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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Cardiac Genetics test prices

Showing 1–4 of 4 matching tests.

Cardiac Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4217 AKAP9 Gene Long QT Syndrome Type 11 Genetic Test This genetic test analyzes the AKAP9 gene to detect variants associated with Long QT syndrome type 11 (LQT11), a condition increasing the risk of cardiac arrhythmias and sudden dea...	Peripheral Whole Blood (EDTA) or Saliva	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AKAP9 gene coding region variants", "Pathogenic variants associated with LQT11"] Parameters [] Preparation ["Maintain current medications unless directed otherwise", "Inform phlebotomist of bleeding disorders or anticoagulant therapy"] Indications ["Diagnosis of Long QT syndrome type 11", "Risk assessment for sudden cardiac death", "Family screening for LQT11"] Measurement technique Confirm with laboratory Codes LOINC: 92884-7 ICD-10: I45.81 Clinical summary This genetic test analyzes the AKAP9 gene to detect variants associated with Long QT syndrome type 11 (LQT11), a condition increasing the risk of cardiac arrhythmias and sudden death.
TEST-4434 MYH6 Gene Atrial Septal Defect Type 3 Genetic Test This test identifies pathogenic variants in the MYH6 gene, which are associated with autosomal dominant atrial septal defect type 3.	Peripheral Whole Blood (3-5 mL) or Buccal Swab	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MYH6 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications"] Indications ["Personal or family history of atrial septal defect, especially diagnosed before age 40"] Measurement technique Confirm with laboratory Codes LOINC: 81319-3 ICD-10: Q21.1 Clinical summary This test identifies pathogenic variants in the MYH6 gene, which are associated with autosomal dominant atrial septal defect type 3.
TEST-3098 NKX2-5 Gene Sequencing for Atrial Septal Defect with AV Conduction Defects Test This test evaluates the NKX2-5 gene for pathogenic variants associated with atrial septal defects and atrioventricular conduction defects.	Whole Blood (EDTA tube), Extracted DNA (≥50 ng/µL), or 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 ["NKX2-5 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed cardiac medications"] Indications ["Pediatric and adult patients with congenital heart disease", "Familial ASD", "Unexplained AV block"] Measurement technique Confirm with laboratory Codes LOINC: 81301-1 ICD-10: Q21.1, I44.30 Clinical summary This test evaluates the NKX2-5 gene for pathogenic variants associated with atrial septal defects and atrioventricular conduction defects.
TEST-4076 TRDN Gene (Catecholaminergic Polymorphic Ventricular Tachycardia Type 5) Genetic Test This test identifies pathogenic variants in the TRDN gene associated with catecholaminergic polymorphic ventricular tachycardia type 5 (CPVT5).	Peripheral whole blood (3-5 mL) 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 the TRDN gene", "Copy Number Variations (CNVs) in the TRDN gene"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "Complete a three-generation pedigree chart"] Indications ["Suspected diagnosis of CPVT5", "Family history of CPVT5 or sudden cardiac death", "Evaluation of unexplained syncope or arrhythmias, especially exercise-induced"] Measurement technique Confirm with laboratory Codes LOINC: 21637-4 ICD-10: I47.2 Clinical summary This test identifies pathogenic variants in the TRDN gene associated with catecholaminergic polymorphic ventricular tachycardia type 5 (CPVT5).

Category overview

Cardiac Genetics: overview

A family history of sudden heart issues or unexplained cardiovascular symptoms warrants proactive insights to protect your lifelong vitality. Representing a core pillar of our specialized Genetics services, Cardiac Genetics testing evaluates your DNA for inherited mutations linked to a wide range of cardiovascular conditions, from complex arrhythmias to structural defects. Utilizing state-of-the-art diagnostic technology, this vital molecular profiling helps uncover hidden risks long before a medical emergency occurs, safely guiding highly personalized cardiac monitoring, preventative lifestyle adjustments, and targeted treatments. Widely respected for specialized cardiovascular diagnostics among top diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, exceptional analytical precision, and incredibly efficient reporting. Safeguard your heart’s future—schedule your cardiac genetics testing in UAE, coordinate a comfortable home sample collection, or connect with our specialized cardiology 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.