Comprehensive Cardiology panel

Cardiovascular diseases (CVDs) are the leading cause of death globally, taking an estimated 17.9 million lives each year. More than four out of five CVD deaths are due to heart attacks and strokes, and one third of these deaths occur prematurely in people under 70 years of age.1

Our comprehensive cardiology panel offers a targeted analysis of genes associated with major cardiovascular disorders. By utilizing advanced sequencing technologies and variant analysis algorithms, we identify and interpret genetic variants within these genes. These variants provide valuable insights into the underlying molecular mechanisms of heart conditions, helping to identify at-risk individuals, provide accurate diagnoses, predict disease progression, assess prognosis, and guide personalized treatment strategies.

With the results obtained from our cardiology panel, informed decisions can be made regarding preventive measures, therapeutic interventions, and long-term follow-up. This leads to more precise and personalized cardiovascular care, empowering individuals to take proactive steps in managing their heart health.

Conditions Covered

Aortic aneurysm, hereditary thoracic panel Catecholaminergic polymorphic ventricular tachycardia panel
Arrhythmia Congenital heart defects
Arrhythmogenic Right Ventricular Cardiomyopathy Familial hypercholesterolemia
Brugada syndrome Heterotaxy
Cardiomyopathy dilated panel Hypertrophic Cardiomyopathy

Individual conditions are also offered

Clinical utility:

Test specification

Technique Coverage Variant types TAT Sample requirements
NGS 150 - 180X SNP 3 - 4 weeks 2 ml EDTA Blood / 2 ug DNA