iGene Cardiac Panel
Heart disease is listed by the CDC as the leading cause of death. Many cardiac diseases have multifactorial causes, but research indicates that genetic predispositions play an important role in the etiology of cardiac disorders. A mutation in a single gene may be associated with several clinical presentations, and mutations in different genes may attribute to similar phenotypes. Next-Generation Sequencing facilitates analysis of multiple genes at the same time and thereby increases the likelihood of detecting potentially pathogenic mutations that may predispose an individual to develop a cardiac disease.
Covered Diseases / Risk Areas: Hypertrophic Cardiomyopathy, Dilated Cardiomyopathy, Arrhythmogenic Right Ventricular Cardiomyopathy, Catecholaminergic Polymorphic Ventricular Tachycardia, Romano-Ward Long QT Syndromes, Brugada Syndromes, Familial Hypercholesterolemia, and Malignant Hyperthermia Susceptibility.
- Genes (23): ACTC1, APOB, COL3A1, DSG2, DSP, GLA, KCNH2, KCNQ1, LDLR, LMNA, MYBPC3, MYH7, MYL3, PCSK9, PKP2, PRKAG2, RYR1, RYR2, SCN5A, TNNI3, TNNT2, TPM1, and TTN
Test Code: 9002
• Confirmation of a clinical diagnosis in symptomatic patients with cardiovascular conditions.
• Risk assessment of asymptomatic family members of patients with cardiovascular conditions
Test Info Sheet: iGene Cardiac Panel
Requisition: General Test Requisition Form
- Turn-Around Time: 4 Weeks
Preferred Specimen: 3-5 mL Whole Blood – Lavender Top Tube
Other Specimens: See details here
- CPT Codes: 81401×1, 81405×5, 81406×10, 81407×3, 81408×2, 81479×2
Pricing: Please contact us at (949) 916-8886 or email@example.com
- Methodology: Next-Generation Sequencing (NGS)
Comprehensive Cardiomyopathy Panel
Familial Hypercholesterolemia Panel
Long QT Syndrome Panel
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