Invitae Amyotrophic Lateral Sclerosis with C9orf72 Panel
Panel analyzes genes associated with ALS, including C9orf72 repeat expansion, the most common genetic cause. Broad testing supports diagnosis, prognosis, and counseling.
Accessed through the ALS Identified Sponsored Testing Program•Sponsored by Biogen•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 ALS Identified Program offers no-charge genetic testing to adults (18+) in the US and Puerto Rico — whether diagnosed with Amyotrophic Lateral Sclerosis (ALS) or with a family history of ALS — to help clarify whether a genetic cause is present. By testing a broad panel of ALS-related genes, the program aims to provide insight into your disease, support family risk assessment, and open doors to potential clinical trials.
Who this may help
Could this be right for you or your family?
- Must be 18 years or older.
- Must reside in the United States or Puerto Rico.
- Must have a diagnosis of ALS, or a family history of ALS (including familial ALS or suspected sporadic ALS, since pathogenic variants may occur even without a known family history).
What to expect
How the process works
- 1
Start Test
Discuss testing with your provider and give consent. Your provider will place the order through Invitae’s online portal.
- 2
Provide a Sample
Your provider will collect your specimen using an Invitae kit and return it using the included shipping label at no additional charge.
- 3
Get Your Results
Access your results online. Your provider can review them with you and use Invitae’s resources to support the discussion.
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 the ALS Identified™ program?
ALS Identified™ is a no-charge genetic testing program for individuals 18 or older in the US or Puerto Rico who have ALS or a family history of ALS. It helps confirm genetic causes and support care planning.
Am I eligible?
You are eligible if you are 18 or older, live in the US or Puerto Rico, and either have a confirmed ALS diagnosis or a family history of ALS — even if your case appears sporadic.
What does the test look for?
The program uses an ALS-focused genetic panel that includes analysis for the C9orf72 hexanucleotide repeat expansion, the most common genetic cause of ALS.
Is there a cost?
No. The test and related services are provided at no charge through the program.
Do I get genetic counseling?
Yes. Individuals in the US tested through the program receive complimentary post-test genetic counseling from Invitae. You can schedule through your patient portal or call Invitae Client Services at 1-800-436-3037.
How will I receive my results?
Results are delivered through your secure Invitae portal. Your healthcare provider will review them with you and help discuss next steps.
Questions to ask your doctor about Invitae Amyotrophic Lateral Sclerosis with C9orf72 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
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