Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel
Comprehensive genetic test evaluating key genes linked to inherited arrhythmias and cardiomyopathies. Helps clarify diagnosis, guide management, and assess familial risk.
Accessed through the Invitae Unlock™ Sponsored Testing Program•Sponsored by Invitae | Labcorp•Performed by Invitae | Labcorp
Designed to help patients understand the purpose of testing and what to expect.
For patients
What this test and program do
The Invitae Unlock™ program provides no-charge genetic testing for individuals in the U.S. who may have an inherited cardiomyopathy or arrhythmia. The test can help clarify whether symptoms or family history may be linked to a genetic cause. Patients who meet eligibility criteria can receive testing ordered by their healthcare provider at no cost.
Who this may help
Could this be right for you or your family?
- You must live in the United States.
- You must have symptoms or a suspected diagnosis of a familial cardiomyopathy or inherited arrhythmia.
- Postmortem testing is not available through this program.
What to expect
How the process works
- 1
Submit an order
Your healthcare provider will place the genetic test order online or using a paper form and include your insurance information.
- 2
Collect specimen
You’ll provide a blood, saliva, or cheek swab sample using a collection kit.
- 3
Receive results
Results are typically available 10–21 days after the lab receives your sample. Your provider will review them with you.
Cost & coverage
Understanding potential costs
If you qualify for this program, the sponsor works with the laboratory to help make testing more affordable. Many patients pay little or no out-of-pocket cost. Your exact cost will depend on your insurance coverage and the specific criteria of the program, and the lab can explain what to expect before your sample is processed.
Quality & privacy
How your sample and information are handled
Testing is performed by Invitae | Labcorp, a CLIA-certified laboratory (CLIA 05D2040778). Your sample is processed using validated methods and quality controls to support reliable genetic results.
Your health information is handled under privacy and security practices that are intended to align with applicable regulations. For program- and lab-specific details, review the privacy information provided by the laboratory and sponsor.
FAQ
Common questions about this program
What is this genetic testing program for?
This program offers no-charge genetic testing for people in the U.S. who may have an inherited cardiomyopathy or arrhythmia. It helps determine whether symptoms or family history could be linked to a genetic cause.
Who is eligible for testing?
You may be eligible if you live in the U.S. and your provider suspects an inherited cardiomyopathy or arrhythmia based on symptoms, test results, or family history. Postmortem testing is not available.
How do I get tested?
Your healthcare provider must order the test. You will provide a blood, saliva, or cheek-swab sample depending on what the provider selects.
Does the program really have no cost?
Yes. If insurance does not cover the test, a sponsored, no-charge option may be available. Your provider will guide you through this process.
How long does it take to get results?
Results are typically available 10–21 days after the lab receives your sample.
Will I receive genetic counseling?
Genetic counseling is not included for patients; however, laboratory genetic counselors are available to assist ordering providers with interpretation.
Can this test help my family members?
If a genetic variant is found, it may help relatives understand their own risks. Your provider can recommend appropriate follow-up.
Questions to ask your doctor about Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel
- Do you think this test is appropriate for me based on my symptoms and history?
- How could the results of this test change my diagnosis or treatment plan?
- What are the potential limitations of this test that I should understand?
- Should any of my family members also be tested based on my results?
- How will we follow up after the results are available?
Notes
See an issue with this program?