Genetics
Cardiovascular Genetics Tests in Dubai & UAE
Investigations in this area, with the specimen type, turnaround time and listed price for each option — so you and your clinician can compare before you book.
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Cardiovascular Genetics investigations
All 39 investigations in this category are listed below.
| Test | What it measures | Specimen | Turnaround | Price | Book |
|---|---|---|---|---|---|
| ACTC1 Gene Atrial Septal Defect Type 5 Genetic Test TEST-4430 LOINC 91847-1 | 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 | Details |
| ALDH1A2 Gene Tetralogy of Fallot Genetic Test TEST-4098 LOINC 94735-5 | 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 | Details |
| BAG3 Gene Dilated Cardiomyopathy (Type 1HH) Genetic Test TEST-4328 LOINC 91628-8 | 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 | Details |
| CACNA1C Gene Brugada Syndrome Type 3 Genetic Test TEST-4409 LOINC 21636-6 | 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 | Details |
| CACNA1C Gene Long QT Syndrome Type 8 Genetic Test TEST-4171 LOINC 77991-4 | 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 | Details |
| Cardiology NGS Genetic Panel Test TEST-4471 LOINC 90270-6 | This test evaluates genetic variations in over 200 genes linked to inherited cardiovascular conditions. | Whole blood (Peripheral) | 3–4 weeks | 3,000.00 AED | Details |
| CNOT3 Gene Cardiac Defects Genetic Test TEST-4376 LOINC 81247-9 | This test evaluates the entire coding region of the CNOT3 gene for pathogenic variants associated with congenital heart defects using Next-Generation... | Peripheral Whole Blood (FTA card also accepted) | 3–4 Weeks | 2,800.00 AED | Details |
| COX15 Gene Sequencing for Fatal Infantile Cardioencephalomyopathy (Cytochrome c Oxidase Deficiency Type 2) Test TEST-4366 LOINC 94196-5 | 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 | Details |
| DSG2 Gene Dilated Cardiomyopathy Type 1BB Genetic Test TEST-4365 LOINC 92784-0 | 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 | Details |
| DTNA Gene Left Ventricular Noncompaction 1 (LVNC1) with or without Congenital Heart Defects Genetic Test TEST-4196 LOINC 51966-3 | 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 | Details |
| GATA4 Gene Ventricular Septal Defect Type 1 Genetic Test TEST-4120 LOINC 77950-1 | 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 | Details |
| GATA5 Gene Congenital Heart Defects, Multiple Types Genetic Test TEST-4252 LOINC 81321-5 | 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 | Details |
| GATA6 Gene Test TEST-4095 LOINC 81320-5 | 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 | Details |
| Genetic Mapping for Cardiovascular Disorders Test TEST-1337 LOINC 53039-4 | 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 | Details |
| JUP Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 12 Genetic Test TEST-4458 LOINC 82207-7 | 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 | Details |
| KCNA5 Gene Atrial Fibrillation Type 7 Genetic Test TEST-4411 LOINC 55233-1 | This genetic test identifies pathogenic variants in the KCNA5 gene associated with familial atrial fibrillation type 7. | Peripheral whole blood | 3-4 weeks from sample receipt | 2,800.00 AED | Details |
| KCNE1 Gene Long QT Syndrome Type 5 Genetic Test TEST-4175 LOINC 81313-1 | This test identifies pathogenic variants in the KCNE1 gene associated with Long QT Syndrome Type 5. | Peripheral whole blood, extracted DNA, or FTA card | 3–4 weeks | 2,800.00 AED | Details |
| KCNE2 Gene Atrial Fibrillation Type 4 Genetic Test TEST-4418 LOINC 55233-1 | This test evaluates the KCNE2 gene for pathogenic variants associated with hereditary atrial fibrillation type 4. | Whole Blood (EDTA), Extracted DNA, or FTA Card Blood Spot | 3–4 Weeks | 2,800.00 AED | Details |
| KCNE3 Gene Brugada Syndrome Type 6 Genetic Test TEST-4383 LOINC 55233-1 | This genetic test evaluates the KCNE3 gene for pathogenic variants associated with Brugada syndrome type 6. | Whole Blood (Peripheral) – EDTA tube | 3 to 4 weeks | 2,800.00 AED | Details |
| KCNH2 Gene Short QT Syndrome Type 1 Genetic Test TEST-4149 LOINC 81208-1 | This test evaluates the KCNH2 gene for pathogenic variants associated with Short QT Syndrome Type 1. | Whole Blood (EDTA), Extracted DNA (≥2 µg), or FTA Card | 3 – 4 Weeks | 2,800.00 AED | Details |
| KCNJ2 Gene Short QT Syndrome Type 3 (SQT3) Genetic Test TEST-4145 LOINC 92076-6 | This test evaluates the KCNJ2 gene for pathogenic variants associated with Short QT Syndrome Type 3 (SQT3), a rare inherited cardiac condition. | Peripheral whole blood (or dried blood spot) | 3–4 Weeks | 2,800.00 AED | Details |
| KCNJ5 Gene Long QT Syndrome Type 13 Genetic Test TEST-4214 LOINC 21662-5 | This genetic test identifies pathogenic variants in the KCNJ5 gene associated with Long QT syndrome type 13. | Peripheral Whole Blood | 3 to 4 Weeks | 2,800.00 AED | Details |
| KCNQ1 Gene Atrial Fibrillation Type 3 Genetic Test TEST-4442 LOINC 80305-0 | This test evaluates the KCNQ1 gene for pathogenic variants associated with hereditary atrial fibrillation type 3. | Whole Blood (EDTA), Extracted DNA, or FTA card | 3–4 weeks | 2,800.00 AED | Details |
| KCNQ1 Gene Jervell and Lange-Nielsen Syndrome Type 1 Genetic Test TEST-4201 LOINC 94477-3 | This genetic test identifies pathogenic mutations in the KCNQ1 gene associated with Jervell and Lange-Nielsen Syndrome (JLNS), a form of long QT syndr... | Peripheral Blood (EDTA Whole Blood), Extracted DNA, or FTA Card | 3-4 Weeks | 2,800.00 AED | Details |
| LMNA Gene Cardiomyopathy (Dilated Type 1A) Genetic Test TEST-4370 LOINC 82248-7 | This genetic test identifies pathogenic variants in the LMNA gene associated with dilated cardiomyopathy type 1A. | Peripheral Whole Blood (3–5 mL in EDTA tube) or DNA FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| LPA Gene Coronary Artery Disease Susceptibility (Genetic Test) TEST-6282 LOINC 21663-7 | This genetic test evaluates the LPA gene for variants associated with elevated lipoprotein(a) levels, a known independent risk factor for premature co... | Whole Blood (Peripheral Venipuncture) | 3–4 Weeks | 2,800.00 AED | Details |
| MAT2A Gene Familial Thoracic Aortic Aneurysm DNA Test TEST-4051 LOINC 96458-9 | This test evaluates the MAT2A gene for pathogenic variants linked to familial thoracic aortic aneurysm risk. | Peripheral Whole Blood (EDTA), Extracted DNA, or FTA Card Dried Blood Spot | 3 to 4 weeks | 2,800.00 AED | Details |
| MED13L Gene Transposition of the Great Arteries, Dextro‑looped 1 Genetic Test TEST-4123 LOINC 94534-9 | This test identifies pathogenic variants in the MED13L gene associated with dextro-looped transposition of the great arteries (d-TGA). | Peripheral whole blood (3–5 mL in EDTA tube) | 21–28 calendar days | 2,800.00 AED | Details |
| MYH6 Gene Dilated Cardiomyopathy Type 1EE Genetic Test TEST-4354 LOINC 90569-1 | This genetic test identifies pathogenic variants in the MYH6 gene, which are linked to dilated cardiomyopathy type 1EE. | Whole Blood (3-5 mL), Extracted DNA, or FTA Card | 3 - 4 Weeks | 2,800.00 AED | Details |
| PPP1R8 Gene Cardiac Defects Genetic Test TEST-4393 LOINC 55233-1 | This test identifies pathogenic variants within the PPP1R8 gene associated with inherited cardiac conditions like cardiomyopathies and congenital hear... | Peripheral whole blood | 3–4 Weeks | 2,800.00 AED | Details |
| PRKAG2 Gene Wolff‑Parkinson‑White Syndrome Genetic Test TEST-4109 LOINC 94219-5 | 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 | Details |
| RYR2 Gene Genetic Test for Arrhythmogenic Right Ventricular Dysplasia Type 2 TEST-4450 LOINC 69548-6 | 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 | Details |
| RYR2 Gene NGS Test for Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 (CPVT1) TEST-4116 LOINC 81395-2 | This test evaluates the RYR2 gene for pathogenic variants associated with Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 (CPVT1). It ide... | Whole Blood (EDTA) or FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| SCN1B Gene Familial Atrial Fibrillation Type 13 Genetic Test TEST-4237 LOINC 51966-2 | 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 | Details |
| SCN5A Gene (Atrial Fibrillation Type 10) Genetic Test TEST-4427 LOINC 96413-5 | 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 | Details |
| SCN5A Gene Brugada Syndrome Type 1 Genetic Test TEST-4413 LOINC 94437-2 | 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 | Details |
| SCN5A Gene Complete NGS Analysis (Progressive Familial Heart Block Type IA) Test TEST-4205 LOINC 95349-4 | 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 | Details |
| SCN5A Gene Sudden Infant Death Syndrome Susceptibility Genetic Test TEST-4137 LOINC 81247-9 | 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 | Details |
| TGFB3 Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 Genetic Test TEST-4443 LOINC 55233-1 | This genetic test analyzes the TGFB3 gene for variants associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1). It identifies m... | Whole Blood, Extracted DNA, Dried Blood Spot (FTA Card) | 3–4 Weeks | 2,800.00 AED | Details |
Clinical overview
About Cardiovascular Genetics
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 your appointment
Preparation & sample collection
Follow the instructions you are given
Fasting, timing and medicine restrictions differ between investigations. The instructions for your specific request are confirmed when you book.
Bring your identification
A valid photo ID is required at collection so that your sample is matched correctly to your record.
Tell us about medicines
Prescription medicines, supplements and recent procedures can affect how an investigation is scheduled or interpreted — please mention them.
Ask before collection
If anything about preparation is unclear, contact us before your appointment. Preparation errors can affect reporting times.
Patient information
Frequently asked questions
Practical answers about Cardiovascular Genetics testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.
How do I choose the right Cardiovascular Genetics test?
The correct investigation depends on what your clinician is trying to establish. Review the specimen type and turnaround time below, then confirm the choice with your treating doctor before booking.
What specimen is required?
Specimen requirements are listed for each investigation. If a request involves more than one sample type, our team will confirm what is needed at the time of booking.
Do you offer home sample collection in Dubai and the UAE?
Yes. Home collection can be arranged across Dubai and the wider UAE. Availability and appointment windows vary by location, so please confirm when you book.
How long do results take?
Turnaround depends on the investigation and the method used. The expected reporting time is confirmed with you before collection.
Is there anything I need to do before sample collection?
Some investigations require fasting, a specific collection time, or avoiding certain medicines or activities. Preparation details are shared when you book — please follow them and ask if anything is unclear.
How will I receive my report?
Reports are issued as secure digital documents and can be shared with your referring clinician on request. Please review results with a qualified clinician who can interpret them in context.
About this clinical information
The information on this Cardiovascular Genetics page describes laboratory investigations in general terms. It is written to help you understand what an investigation involves — it is not a diagnosis and it is not a substitute for advice from your treating clinician.
- Investigation names, specimen types and listed prices are reviewed against laboratory records.
- Preparation guidance is indicative — confirm test-specific instructions before collection.
- Content is updated when investigations, methods or reporting formats change.
- Results are released to the patient and, on request, shared with the referring clinician.
Medical disclaimer: This page is for general information and education only. It is not medical advice, diagnosis or treatment, and it does not replace a consultation with a qualified healthcare professional. Always seek the advice of your doctor or another qualified provider with any questions about a medical condition or before ordering a test.
We're here to help
Need help choosing a Cardiovascular Genetics test?
Tell us what your clinician has requested and we'll confirm availability, price, preparation and the most convenient collection option — including home collection in Dubai and across the UAE.
- Home collection available across the UAE
- Digital reports delivered securely
- Confidential handling of every request
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