Analyses 168 genes associated with inherited arrhythmias and cardiomyopathies to identify clinically relevant genetic variants affecting heart rhythm or heart-muscle function.
Used to investigate suspected inherited heart conditions, particularly in people with cardiomyopathy, an abnormal heart rhythm, unexplained fainting or cardiac arrest, or a family history of inherited heart disease or sudden cardiac death. Results may support diagnosis, clinical management, genetic counselling and targeted testing of biological relatives.