Cardiovascular Genetic Testing

Unlock the Power of Your Genes to Protect Your Heart

Cardiovascular genetic testing helps identify inherited risks for heart diseases, allowing for early intervention, personalized treatments, and proactive management of your heart health.

Why Choose Cardiovascular Genetic Testing?

  • Early Detection: Identify inherited heart conditions before symptoms appear.
  • Personalized Treatment Plans: Tailor medications and lifestyle choices based on genetic predisposition.
  • Family Screening: Understand hereditary risks and help family members take preventive steps.
  • Risk Assessment: Determine susceptibility to conditions like coronary artery disease, arrhythmias, and cardiomyopathies.

Who Should Consider This Test?

  • Individuals with a family history of heart disease, sudden cardiac arrest, or unexplained fainting.
  • Patients with early-onset heart disease (before age 55 for men, 65 for women).
  • Those diagnosed with cardiomyopathy, arrhythmia, or high cholesterol at a young age.
  • People with unexplained strokes or blood clotting disorders.

Conditions We Screen For

  • Aorta Panel
  • Arrhythmia Panel
  • Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Panel
  • Atrial Fibrillation Panel
  • Brugada Syndrome Panel
  • Cardiomyopathy Panel
  • Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel
  • Comprehensive Cardiology Panel
  • Congenital Structural Heart Disease Panel
  • Dilated Cardiomyopathy (DCM) Panel
  • Ehlers-Danlos Syndrome Panel
  • Hereditary Hemorrhagic Telangiectasia (HHT) Panel
  • Heterotaxy and Situs Inversus Panel
  • Hyperlipidemia Core Panel
  • Hyperlipidemia Panel
  • Hypertrophic Cardiomyopathy (HCM) Panel
  • Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel
  • Liddle Syndrome Panel
  • Long QT Syndrome (LQTS) Panel
  • Marfan Syndrome Panel
  • Noonan Syndrome Panel
  • Pulmonary Artery Hypertension (PAH) Panel
  • Short QT Syndrome (SQTS) Panel

Comprehensive Genes List

A4GALT, A4GNT, AAAS, AADAC, AADACL2, AAGAB, AANAT, AARS, AARS2, AASS, ABAT, ABCA1, ABCA10, ABCA12, ABCA13, ABCA2, ABCA3, ABCA4, ABCA5, ABCA7, ABCB1, ABCB11, ABCB4, ABCB5, ABCB6, ABCB7, ABCC1, ABCC11, ABCC12, ABCC2, ABCC3, ABCC4, ABCC6, ABCC8, ABCC9, ABCD1, ABCD3, ABCD4, ABCG1, ABCG2, ABCG5, ABCG8, ABHD1, ABHD12, ABHD5, ABI3BP, ABL1, ABL2, ABO, ABRAXAS1, ACACA, ACACB, ACAD10, ACAD11, ACAD8, ACAD9, ACADL, ACADM, ACADS, ACADSB, ACADVL, ACAN, ACAT1, ACAT2, ACBD5, ACBD6, ACCS, ACE, ACHE, ACKR1, ACKR3, ACLY, ACMSD, ACO2, ACOX1, ACP1, ACP2, ACP5, ACP6,

How It Works?

1. Consultation: Discuss your medical history and risks with a genetic counselor.
2. Sample Collection: Provide a saliva or blood sample for DNA analysis.
3. Comprehensive Genetic Analysis: Advanced testing detects key genetic mutations.
4. Personalized Report: Receive a detailed report with actionable insights.
5. Expert Guidance: Work with a specialist to interpret results and plan next steps.

Why Choose Us?

  • Advanced Testing Technology: Cutting-edge genetic sequencing for precise results.
  • Certified Specialists: Genetic counsellors and cardiologists to guide you.
  • Privacy & Security: Your data is protected with strict confidentiality policies.
  • Fast & Reliable Results: Get insights within a few weeks.