Cardiovascular Genetics tests in Dubai & UAE

Compare available Cardiovascular 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

2,300.00–3,000.00 AED

Clinical preparation

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Cardiovascular Genetics test prices

Showing 31–39 of 39 matching tests.

Cardiovascular Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4109 PRKAG2 Gene Wolff‑Parkinson‑White Syndrome Genetic Test This test evaluates the PRKAG2 gene for variants associated with Wolff‑Parkinson‑White syndrome and glycogen storage cardiomyopathies.	Whole Blood (EDTA)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PRKAG2 gene variants", "SNVs", "Indels", "CNVs"] Parameters [] Preparation ["No fasting required."] Indications ["Diagnosis confirmation of WPW syndrome", "Identification of genetic cause of glycogen storage cardiomyopathy", "Family screening for PRKAG2-related conditions"] Measurement technique Confirm with laboratory Codes LOINC: 94219-5 ICD-10: I45.6, I42.7 Clinical summary This test evaluates the PRKAG2 gene for variants associated with Wolff‑Parkinson‑White syndrome and glycogen storage cardiomyopathies.
TEST-4450 RYR2 Gene Genetic Test for Arrhythmogenic Right Ventricular Dysplasia Type 2 This test identifies pathogenic variants in the RYR2 gene associated with Arrhythmogenic Right Ventricular Dysplasia Type 2 (ARVD2).	Peripheral Whole Blood or Extracted DNA (FTA card acceptable)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in RYR2 gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting physician"] Indications ["Diagnosis of suspected ARVD2", "Family cascade screening for ARVD2", "Risk stratification for sudden cardiac death", "Personalized cardiac risk management"] Measurement technique Confirm with laboratory Codes LOINC: 69548-6 ICD-10: I42.8, I47.2, Z15.89 Clinical summary This test identifies pathogenic variants in the RYR2 gene associated with Arrhythmogenic Right Ventricular Dysplasia Type 2 (ARVD2).
TEST-4116 RYR2 Gene NGS Test for Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 (CPVT1) This test evaluates the RYR2 gene for pathogenic variants associated with Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 (CPVT1). It identifies mutations that cause t...	Whole Blood (EDTA) or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RYR2 gene sequence", "Pathogenic variants in RYR2"] Parameters [] Preparation ["No fasting required", "Pre-test hydration is encouraged"] Indications ["Diagnosis of CPVT1", "Risk stratification for CPVT1", "Cascade testing for family members of CPVT1 patients"] Measurement technique Confirm with laboratory Codes LOINC: 81395-2 ICD-10: I47.2 Clinical summary This test evaluates the RYR2 gene for pathogenic variants associated with Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 (CPVT1). It identifies mutations that cause this inherited heart rhythm disorder.
TEST-4237 SCN1B Gene Familial Atrial Fibrillation Type 13 Genetic Test This genetic test evaluates the SCN1B gene for mutations associated with familial atrial fibrillation type 13.	Peripheral Whole Blood (EDTA) or FTA Dried Blood Spot	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SCN1B gene coding region", "Pathogenic single-nucleotide variants", "Small insertions/deletions"] Parameters [{"name": "Analytical Sensitivity", "reference_range": ">99.9% for all coding variants"}] Preparation ["No specific fasting required", "Inform lab if on unstable anticoagulation therapy"] Indications ["Family history suggestive of hereditary cardiac conditions", "Personal history of atrial fibrillation with potential genetic link"] Measurement technique Confirm with laboratory Codes LOINC: 51966-2 ICD-10: I48.91 Clinical summary This genetic test evaluates the SCN1B gene for mutations associated with familial atrial fibrillation type 13.
TEST-4427 SCN5A Gene (Atrial Fibrillation Type 10) Genetic Test This genetic test identifies pathogenic and likely pathogenic variants in the SCN5A gene associated with familial atrial fibrillation type 10.	Peripheral Whole Blood (EDTA) or Buccal Swab	21 to 28 Calendar Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SCN5A gene", "Likely pathogenic variants in the SCN5A gene"] Parameters [] Preparation [] Indications ["Diagnosis of familial atrial fibrillation type 10", "Risk stratification for hereditary arrhythmia syndromes", "Cascade screening for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 96413-5 ICD-10: I48.91, Z15.89 Clinical summary This genetic test identifies pathogenic and likely pathogenic variants in the SCN5A gene associated with familial atrial fibrillation type 10.
TEST-4413 SCN5A Gene Brugada Syndrome Type 1 Genetic Test This test evaluates the SCN5A gene for variants associated with Brugada syndrome type 1, a cardiac channelopathy.	Whole blood (EDTA tube), extracted genomic DNA, or FTA card blood spot	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SCN5A gene sequence", "Pathogenic variants", "Likely pathogenic variants", "Copy number alterations"] Parameters [] Preparation [] Indications ["Diagnosis of Brugada syndrome type 1", "Family cascade screening", "Risk stratification for sudden cardiac death", "Guiding ICD implantation decisions"] Measurement technique Confirm with laboratory Codes LOINC: 94437-2 ICD-10: I49.81 Clinical summary This test evaluates the SCN5A gene for variants associated with Brugada syndrome type 1, a cardiac channelopathy.
TEST-4205 SCN5A Gene Complete NGS Analysis (Progressive Familial Heart Block Type IA) Test This test identifies pathogenic variants within the SCN5A gene associated with progressive familial heart block type IA.	Peripheral whole blood (3 mL EDTA)	21 calendar days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DNA sequence variants in the SCN5A gene", "Copy number changes in the SCN5A gene"] Parameters [] Preparation ["No fasting required", "Provide detailed family cardiac history", "Provide signed genetic counselling consent"] Indications ["Diagnosis of progressive familial heart block type IA", "Family screening for SCN5A-related heart block", "Risk assessment in individuals with unexplained syncope or heart block"] Measurement technique Confirm with laboratory Codes LOINC: 95349-4 ICD-10: I45.5 Clinical summary This test identifies pathogenic variants within the SCN5A gene associated with progressive familial heart block type IA.
TEST-4137 SCN5A Gene Sudden Infant Death Syndrome Susceptibility Genetic Test This genetic test evaluates the SCN5A gene for variants associated with sudden infant death syndrome, Brugada syndrome, and long-QT syndrome type 3.	Whole Blood (3 mL EDTA), Extracted DNA (≥1 μg), or FTA Card blood spot	3–4 weeks (urgent results in 10 days upon request)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SCN5A gene variants", "Coding exons", "Splice-site regions", "Copy-number changes"] Parameters [{"name": "Diagnostic Precision", "reference_range": "99.9% sensitivity via full gene NGS (coverage >100x, allelic depth confirmed by orthogonal methods)"}] Preparation ["Complete a genetic counseling session", "Provide pedigree documentation", "Follow specific pre-preparation guidelines if advised during counseling"] Indications ["Family history of sudden infant death", "Family history of Brugada syndrome", "Family history of long-QT syndrome type 3", "Evaluation of unexplained infant loss"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Z13.71 Clinical summary This genetic test evaluates the SCN5A gene for variants associated with sudden infant death syndrome, Brugada syndrome, and long-QT syndrome type 3.
TEST-4443 TGFB3 Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 Genetic Test This genetic test analyzes the TGFB3 gene for variants associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1). It identifies mutations linked to an inherite...	Whole Blood, Extracted DNA, 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 ["Single-nucleotide variants in TGFB3 gene", "Small insertions or deletions in TGFB3 gene", "Exon-level copy number changes in TGFB3 gene"] Parameters [] Preparation [] Indications ["Clinical suspicion of Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1)", "Family history of ARVC1", "Cascade screening of at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: I42.8 Clinical summary This genetic test analyzes the TGFB3 gene for variants associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1). It identifies mutations linked to an inherited heart muscle disorder increasing risk for arrhythmias and sudden cardiac arrest.

Category overview

Cardiovascular Genetics: overview

A family history of sudden heart issues or unexplained cardiovascular symptoms warrants proactive insights to protect your lifelong vitality before a medical emergency occurs. Representing a core pillar of our specialized Genetics services, Cardiovascular Genetics testing evaluates your DNA for inherited mutations linked to a wide range of cardiovascular conditions, from complex arrhythmias to structural defects like familial hypercholesterolemia. Utilizing state-of-the-art diagnostic technology, this vital molecular profiling helps uncover hidden risks, 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 cardiovascular genetics testing in UAE, coordinate a comfortable home sample collection, or connect with our specialized cardiology team.

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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.