Invitae Spinal Muscular Atrophy STAT Panel
Test analyzes SMN1 copy number to diagnose SMA and reports SMN2 copies when SMN1 is deleted. A rapid 4-day STAT TAT supports urgent treatment decisions.
Accessed through the SMA 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
Getting a clear genetic answer matters when spinal muscular atrophy (SMA) is suspected, because confirming a diagnosis can open the door to timely treatment conversations with your doctor. The SMA Identified program, sponsored by Biogen, provides genetic testing at no cost to you or your family. The program can also help determine carrier status for those with a family history of SMA. Biogen covers the full cost of testing and never receives any information that could identify you personally.
Who this may help
Could this be right for you or your family?
- Patients in the US and Puerto Rico may qualify if they have a suspected diagnosis of spinal muscular atrophy (SMA) or a family history of SMA. Eligibility includes individuals who:
- Are suspected of having SMA or were diagnosed with SMA but do not know their SMN2 copy number
- Are undiagnosed but have a family history of SMA
- Are a first-degree relative of someone diagnosed with SMA through genetic testing
What to expect
How the process works
- 1
Start Order
Discuss testing with your provider and give consent. Your provider will place the order through Invitae’s online portal.
- 2
Provide Sample
Use the Invitae collection kit to submit your sample. Most US shipments can be returned at no additional charge using the provided label.
- 3
Get Results
View your results online. Your provider will review them with you and discuss next steps.
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 SMA Identified program and how does it help families affected by spinal muscular atrophy?
SMA Identified is a sponsored genetic testing program designed to help people who may have spinal muscular atrophy or who want to know if they carry the gene changes linked to SMA. The program uses a 2-gene panel called the Invitae Spinal Muscular Atrophy STAT Panel, performed by Invitae at Labcorp. Results from SMA Identified can help confirm a diagnosis or clarify carrier status, which can guide important conversations with your healthcare provider about next steps.
Is the SMA Identified genetic test really free, and who pays for it?
Yes, the SMA Identified test is provided at absolutely no cost to you. Biogen, a company focused on neurological diseases, sponsors the program and covers the entire cost of testing. You will not receive a bill, a copay, or any charge for participating in the SMA Identified program.
What kind of sample is needed for the SMA Identified genetic test?
The SMA Identified program accepts several sample types, including whole blood, saliva, a buccal swab (a gentle cheek swab), or extracted DNA. Your healthcare provider will choose the option that works best for your situation, and a collection kit can be sent directly to their office.
How long does it take to get results from the SMA Identified spinal muscular atrophy test?
Results from the SMA Identified program are typically returned in about 4 days. Because SMA testing can be time-sensitive, especially for infants and young children, this fast turnaround is designed to help families and their doctors move forward with care decisions as quickly as possible.
Is genetic counseling available through the SMA Identified program?
Yes, genetic counseling is available through the SMA Identified program at no cost to you. A genetic counselor can help you understand your results, explain what they mean for your family, and support you in discussing next steps with your doctor. This service is available to participants in the United States.
Does participating in SMA Identified require me to take any medication or buy anything?
No. Participating in the SMA Identified program does not require you to purchase, use, or support any product or medication. The program is simply a way to access genetic testing for spinal muscular atrophy at no cost. If your results are positive, your healthcare provider can discuss any treatment options that may be appropriate for you.
Who qualifies for SMA Identified Spinal Muscular Atrophy genetic testing?
Patients may qualify for SMA Identified if they meet the program's eligibility criteria:
- Patients in the US and Puerto Rico may qualify if they have a suspected diagnosis of spinal muscular atrophy (SMA) or a family history of SMA. Eligibility includes individuals who:
- Are suspected of having SMA or were diagnosed with SMA but do not know their SMN2 copy number
- Are undiagnosed but have a family history of SMA
- Are a first-degree relative of someone diagnosed with SMA through genetic testing
Questions to ask your doctor about Invitae Spinal Muscular Atrophy STAT 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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