Cardiac Genetic Testing
What is cardiac genetic risk assessment and testing?
Cardiac risk assessment is the process your healthcare provider uses to understand how likely you are to develop heart problems, such as a heart attack or other heart disease. It involves looking at your personal health, lifestyle, and family history to identify any factors that might increase your risk. If the genetic expert determines testing is appropriate for you, a simple blood test or mouth swab will be collected. This test looks at your DNA to find inherited changes that may increase your risk for certain heart conditions. Many of these conditions can run in families, even if no one has been diagnosed before.
Who should consider testing?
Your physician or advanced practice provider may recommend testing if you:
- Have a personal or family history of heart disease at a young age
- Have been diagnosed with a heart rhythm disorder or cardiomyopathy
- Have a family member with a known genetic heart condition
- Have experienced unexplained fainting or cardiac events
What to expect:
- A simple blood or saliva test
- No special preparation needed
- Results typically available within a few weeks
- Guidance from your care team to understand your results
Why it matters:
- Detects risk before symptoms begin
- Helps guide personalized care and treatment
- Provides important information for your family members
- Supports early intervention to prevent serious complications
If you’re concerned about your heart health or family history, talk with your provider about cardiac genetic risk assessment and testing at SOMC. Patients need a referral from a healthcare provider before genetic risk assessment and testing is performed.
