Genetic Full Cardiac Risk
A comprehensive genetic screening panel assessing variants linked with inherited cardiac conditions. It supports assessment of genetic causes of cardiomyopathy, inherited heart-rhythm disorders and other conditions associated with sudden cardiac death.
What does it check?
- Genes associated with inherited cardiomyopathies
- Genes associated with inherited arrhythmia syndromes
- Genes linked with inherited cardiac conditions and sudden cardiac-death risk
Who may benefit?
This test may be appropriate for people with suspected or confirmed inherited cardiac disease, unexplained cardiac symptoms, a personal history of cardiomyopathy or arrhythmia, or a family history of early cardiac disease or sudden cardiac death.
Genetic Full Cardiac Risk
What is it?
A comprehensive genetic screening panel assessing variants linked with inherited cardiac conditions. It supports assessment of genetic causes of cardiomyopathy, inherited heart-rhythm disorders and other conditions associated with sudden cardiac death.
Who may benefit?
This test may be appropriate for people with suspected or confirmed inherited cardiac disease, unexplained cardiac symptoms, a personal history of cardiomyopathy or arrhythmia, or a family history of early cardiac disease or sudden cardiac death.
Important information
This is a genetic risk and diagnostic-support test. A result must be interpreted by an appropriately qualified clinician alongside symptoms, ECG or imaging findings, personal history and family history. A negative result does not exclude every inherited cardiac condition; specialist cardiology or genetics referral may be recommended.