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

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Cardiovascular Genetics test prices

Showing 1–15 of 39 matching tests.

Cardiovascular Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4430 ACTC1 Gene Atrial Septal Defect Type 5 Genetic Test This test identifies mutations in the ACTC1 gene associated with Atrial Septal Defect Type 5.	Whole Blood	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Mutations in the ACTC1 gene", "Cardiac actin gene variants"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue cardiac medication"] Indications ["Diagnosis of Atrial Septal Defect Type 5", "Family cascade screening", "Personalized cardiac management", "Pre-implantation genetic diagnosis (PGD) counseling"] Measurement technique Confirm with laboratory Codes LOINC: 91847-1 ICD-10: Q21.1 Clinical summary This test identifies mutations in the ACTC1 gene associated with Atrial Septal Defect Type 5.
TEST-4098 ALDH1A2 Gene Tetralogy of Fallot Genetic Test This test identifies pathogenic variants in the ALDH1A2 gene associated with Tetralogy of Fallot.	Peripheral whole blood (EDTA tube)	3–4 weeks (21–28 days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ALDH1A2 gene", "DNA sequence analysis of the ALDH1A2 gene"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed unless advised by physician"] Indications ["Diagnosis of Tetralogy of Fallot", "Risk assessment for familial inheritance", "Prenatal diagnosis", "Pre-surgical planning"] Measurement technique Confirm with laboratory Codes LOINC: 94735-5 ICD-10: Q21.3 Clinical summary This test identifies pathogenic variants in the ALDH1A2 gene associated with Tetralogy of Fallot.
TEST-4328 BAG3 Gene Dilated Cardiomyopathy (Type 1HH) Genetic Test This genetic test evaluates for pathogenic variants in the BAG3 gene associated with dilated cardiomyopathy type 1HH.	Whole Blood (peripheral), 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 BAG3 gene", "Copy Number Variations (CNVs) in the BAG3 gene"] Parameters [] Preparation [] Indications ["Diagnosis confirmation of dilated cardiomyopathy type 1HH", "Familial risk assessment", "Guiding precision management"] Measurement technique Confirm with laboratory Codes LOINC: 91628-8 ICD-10: I42.0 Clinical summary This genetic test evaluates for pathogenic variants in the BAG3 gene associated with dilated cardiomyopathy type 1HH.
TEST-4409 CACNA1C Gene Brugada Syndrome Type 3 Genetic Test This test identifies pathogenic variants in the CACNA1C gene associated with Brugada syndrome type 3.	Peripheral 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 CACNA1C gene", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)", "Copy number variations (CNVs)", "Splice-site variants"] Parameters [] Preparation ["No fasting required", "No medication adjustments required", "Bring valid Emirates ID", "Complete consent form", "Provide brief clinical history questionnaire", "Inform phlebotomist if taking anticoagulants"] Indications ["Diagnosis of Brugada syndrome type 3", "Risk stratification for sudden cardiac death", "Cascade screening of family members", "Evaluation of unexplained syncope or sudden cardiac death in family history"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: I49.8 Clinical summary This test identifies pathogenic variants in the CACNA1C gene associated with Brugada syndrome type 3.
TEST-4171 CACNA1C Gene Long QT Syndrome Type 8 Genetic Test This test evaluates the CACNA1C gene for pathogenic variants associated with Long QT Syndrome Type 8 (Timothy syndrome).	Whole blood (EDTA), buccal swab, 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 CACNA1C gene", "Coding region and flanking intronic regions of the CACNA1C gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Personal or family history of unexplained sudden cardiac arrest, syncope, or prolonged QT interval on ECG", "Asymptomatic relatives of a confirmed Timothy syndrome patient", "Competitive athletes undergoing pre-participation cardiac screening", "Families planning pregnancy when one partner carries a known CACNA1C variant"] Measurement technique Confirm with laboratory Codes LOINC: 77991-4 ICD-10: I45.81 Clinical summary This test evaluates the CACNA1C gene for pathogenic variants associated with Long QT Syndrome Type 8 (Timothy syndrome).
TEST-4471 Cardiology NGS Genetic Panel Test This test evaluates genetic variations in over 200 genes linked to inherited cardiovascular conditions.	Whole blood (Peripheral)	3–4 weeks	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Continue prescribed medications unless advised otherwise by your physician"] Indications ["Assessment of risk for inherited cardiomyopathies", "Evaluation of familial hypercholesterolemia", "Screening for long QT syndrome", "Investigation of unexplained sudden cardiac death in family"] Measurement technique Confirm with laboratory Codes LOINC: 90270-6 ICD-10: Z13.6 Clinical summary This test evaluates genetic variations in over 200 genes linked to inherited cardiovascular conditions.
TEST-4376 CNOT3 Gene Cardiac Defects Genetic Test This test evaluates the entire coding region of the CNOT3 gene for pathogenic variants associated with congenital heart defects using Next-Generation Sequencing.	Peripheral Whole Blood (FTA card also accepted)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CNOT3 gene coding region", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Maintain current medications unless advised otherwise by a physician"] Indications ["Patients with congenital heart defects", "Family history of CNOT3-related anomalies", "Unexplained congenital heart disease", "Parents planning future pregnancies after a previous affected child", "Cascade testing for first-degree relatives of a confirmed CNOT3 proband"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q24.9, Q21.1, Q21.0 Clinical summary This test evaluates the entire coding region of the CNOT3 gene for pathogenic variants associated with congenital heart defects using Next-Generation Sequencing.
TEST-4366 COX15 Gene Sequencing for Fatal Infantile Cardioencephalomyopathy (Cytochrome c Oxidase Deficiency Type 2) Test This test detects pathogenic variants in the COX15 gene associated with fatal infantile cardioencephalomyopathy.	Whole Blood, Extracted DNA, FTA Card Blood Spot	21-28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the COX15 gene", "Copy Number Variations (CNV) in the COX15 gene"] Parameters [] Preparation ["No specific fasting required.", "Inform the phlebotomist of any medications or supplements being taken."] Indications ["Suspected fatal infantile cardioencephalomyopathy", "Family history of COX15 deficiency", "Need for definitive genetic diagnosis for management and counselling"] Measurement technique Confirm with laboratory Codes LOINC: 94196-5 ICD-10: E88.49, I42.8, G93.40 Clinical summary This test detects pathogenic variants in the COX15 gene associated with fatal infantile cardioencephalomyopathy.
TEST-4365 DSG2 Gene Dilated Cardiomyopathy Type 1BB Genetic Test This genetic test identifies mutations in the DSG2 gene associated with dilated cardiomyopathy type 1BB.	Whole Blood or Saliva	21 – 28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DSG2 gene mutations", "Coding region variants", "Splice site variants", "Deep intronic variants"] Parameters [] Preparation [] Indications ["Diagnosis of dilated cardiomyopathy", "Family risk stratification", "Informed clinical management", "Predictive testing in minors (with consent)"] Measurement technique Confirm with laboratory Codes LOINC: 92784-0 ICD-10: I42.0 Clinical summary This genetic test identifies mutations in the DSG2 gene associated with dilated cardiomyopathy type 1BB.
TEST-4196 DTNA Gene Left Ventricular Noncompaction 1 (LVNC1) with or without Congenital Heart Defects Genetic Test This genetic test identifies pathogenic variants in the DTNA gene associated with left ventricular noncompaction (LVNC) and congenital heart defects.	Whole Blood (EDTA), Extracted DNA, Dried Blood Spot (FTA Card)	14-18 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the DTNA gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed cardiac medication without consulting your physician"] Indications ["Diagnosis of LVNC", "Family screening for LVNC", "Risk stratification for cardiac events", "Genotype-phenotype correlation"] Measurement technique Confirm with laboratory Codes LOINC: 51966-3 ICD-10: I42.8, Q24.9 Clinical summary This genetic test identifies pathogenic variants in the DTNA gene associated with left ventricular noncompaction (LVNC) and congenital heart defects.
TEST-4120 GATA4 Gene Ventricular Septal Defect Type 1 Genetic Test This genetic test evaluates the GATA4 gene for pathogenic variants associated with congenital ventricular septal defect type 1.	Peripheral Whole Blood 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 GATA4 gene"] Parameters [] Preparation ["Mandatory genetic counselling session required", "No fasting or medication changes needed"] Indications ["Diagnosis of congenital ventricular septal defect type 1", "Family screening for GATA4-related VSD"] Measurement technique Confirm with laboratory Codes LOINC: 77950-1 ICD-10: Q21.0 Clinical summary This genetic test evaluates the GATA4 gene for pathogenic variants associated with congenital ventricular septal defect type 1.
TEST-4252 GATA5 Gene Congenital Heart Defects, Multiple Types Genetic Test This test analyzes the GATA5 gene for pathogenic variants associated with congenital heart defects.	Peripheral whole blood (or FTA card)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GATA5 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications"] Indications ["Diagnosis of congenital heart defects", "Recurrence risk assessment", "Family screening"] Measurement technique Confirm with laboratory Codes LOINC: 81321-5 ICD-10: Q24.9 Clinical summary This test analyzes the GATA5 gene for pathogenic variants associated with congenital heart defects.
TEST-4095 GATA6 Gene Test This test identifies pathogenic variants in the GATA6 gene associated with congenital heart defects like Tetralogy of Fallot.	Whole Blood (EDTA), Extracted 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 ["Pathogenic variants in the GATA6 gene", "Coding exons ± 20 bp splice junctions"] Parameters [] Preparation ["Avoid eating for three hours prior to collection", "Provide the patient’s latest echocardiogram report during the visit"] Indications ["Reproductive risk assessment", "Surgical prognostication", "Cascade screening of at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 81320-5 ICD-10: Q21.3 Clinical summary This test identifies pathogenic variants in the GATA6 gene associated with congenital heart defects like Tetralogy of Fallot.
TEST-1337 Genetic Mapping for Cardiovascular Disorders Test This test evaluates genetic predispositions to inherited cardiovascular conditions by analyzing SNPs and CNVs.	3 mL Whole Blood (Lavender Top EDTA Tube)	8 Weeks	2,300.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide polymorphisms (SNPs)", "Chromosomal copy number variations (CNVs)", "Genome-wide cardiovascular risk loci"] Parameters [] Preparation ["Inform phlebotomist of all current medications, including anticoagulants, antiplatelet agents, and high-dose omega-3 fatty acid supplements.", "Do not discontinue medication without explicit physician approval.", "Do not adjust, initiate, or stop any prescribed cardiovascular therapy based solely on genetic mapping results."] Indications ["Strong family history of premature heart disease", "Athletes undergoing pre-participation cardiac screening", "Patients with unexplained cardiomyopathy", "Sudden cardiac arrest survivors", "Risk stratification in apparently healthy individuals"] Measurement technique Confirm with laboratory Codes LOINC: 53039-4 ICD-10: I25.10, Z84.1, I42.8 Clinical summary This test evaluates genetic predispositions to inherited cardiovascular conditions by analyzing SNPs and CNVs.
TEST-4458 JUP Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 12 Genetic Test This genetic test identifies pathogenic variants in the JUP gene associated with arrhythmogenic right ventricular cardiomyopathy type 12 (ARVC-12).	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 ["Pathogenic variants in the JUP gene", "Copy Number Variants (CNVs) in the JUP gene"] Parameters [] Preparation [] Indications ["Personal or family history of ARVC", "Unexplained syncope", "Ventricular arrhythmias", "Sudden cardiac death, especially in relatives under 40", "First-degree relatives of known JUP variant carriers"] Measurement technique Confirm with laboratory Codes LOINC: 82207-7 ICD-10: I42.8 Clinical summary This genetic test identifies pathogenic variants in the JUP gene associated with arrhythmogenic right ventricular cardiomyopathy type 12 (ARVC-12).

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.

Before booking

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.