The CardioGxOneTM panel is a comprehensive NGS based molecular test for inherited cardiovascular diseases. The CardioGxOneTM test detects genomic variations in 213 genes related to cardiovascular diseases and provides cardiologists and other physician specialists with clear genetic interpretation for risk assessment and disease diagnosis.
A comprehensive genetic diagnostic test that serves the cardiovascular community.
Provides physicians with expert analysis from a team of leading cardiologists.
CardioGxOne™ provides analysis on a broad spectrum of diseases
Congenital Heart Disease
Channelopathies & Arrhythmias
Cuttting Edge Technology
Advanced Next-Generation sequencing technology and propriety bioinformatics analysis.
28, 000 papers on inherited cardiovascular diseases(400 added monthly).
Approximately 40,000 families.
300,000 genetic variants.
Results by Leading Cardiologists
Clear, accurate and thorough clinical interpretation created by a team of leading cardiologists.
Inherited Cardiovascular Diseases and Sudden Death