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Cardiology / Neurology / MusculoskeletalFriedreich Ataxia (FA)

Friedreich Ataxia Genetic Evaluation

Analyzes the FXN gene for pathogenic variants and GAA repeat expansions associated with Friedreich Ataxia (FA) to support accurate diagnosis and clinical evaluation.

Accessed through the FA Identified Sponsored Testing Program•Sponsored by Biogen•Performed by Prevention Genetics

Designed to help patients understand the purpose of testing and what to expect.

For patients

What this test and program do

Friedreich ataxia (FA) is a rare inherited condition that can affect balance, coordination, and nerve function, and getting a clear genetic answer matters. The FA Identified program, sponsored by Biogen, provides no-cost genetic testing to help determine whether FA is the cause of your symptoms. A healthcare provider places the order on your behalf, and the testing is performed by Prevention Genetics, an established clinical laboratory. You pay nothing for the test itself because Biogen covers the full cost.

Who this may help

Could this be right for you or your family?

  • To qualify, all of the following must be met:
    • The patient lives in the United States or Puerto Rico
    • The patient is suspected of having, or has been diagnosed with, Friedreich Ataxia
    • The patient is 16 years of age or older

What to expect

How the process works

  1. 1

    Confirm Eligibility

    Talk with your provider to see if you meet the program criteria and whether this FA genetic test is appropriate for your evaluation.

  2. 2

    Provider Orders Test

    Your provider will order the test using the test requisition form (TRF) and guide you on what to expect during specimen collection.

  3. 3

    Provide a Specimen

    Your provider will collect and label your specimen using at least two identifiers. Specimens are accepted Monday–Saturday; holiday schedules are posted in advance.

  4. 4

    Receive Your Results

    PreventionGenetics processes your test, and results are typically sent to your provider about three weeks after your sample and paperwork are received.

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 Prevention Genetics, a CLIA-certified laboratory (CLIA 52D2065132) and College of American Pathologists (CAP) certified laboratory (CAP 7185561). 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 FA Identified genetic testing program for Friedreich ataxia?

FA Identified is a sponsored genetic testing program focused on Friedreich ataxia (FA). It is designed to help people who may have FA get a clear genetic answer about their diagnosis. The program is sponsored by Biogen, and the test is performed by Prevention Genetics, a certified clinical laboratory. A healthcare provider must order the test on your behalf.

Is the FA Identified Friedreich ataxia genetic test really free?

Yes, the FA Identified program is completely free to you. Biogen, the program's sponsor, covers the full cost of the genetic testing. You will not receive a bill, and there is no copay or deductible. Your only step is to work with a healthcare provider who can place the order.

What kind of sample is needed for the Friedreich ataxia genetic test?

The FA Identified program accepts a whole blood draw, a saliva sample, or a buccal swab (a gentle cheek swab). Your healthcare provider will help determine which option works best for you. A sample collection kit is sent to your provider's office to make the process straightforward.

How long does it take to get results from the FA Identified Friedreich ataxia test?

Results from the FA Identified program are typically available within 2 to 3 weeks after the lab receives your sample. Your ordering healthcare provider will share the results with you and can help explain what they mean for your care.

Do I need a doctor to order the FA Identified Friedreich ataxia genetic test?

Yes, the FA Identified genetic test for Friedreich ataxia must be ordered by a qualified healthcare provider. You cannot order it on your own. If you think you may benefit from testing, talk to your doctor or a specialist about whether the program is right for you.

Is genetic counseling available through the FA Identified Friedreich ataxia testing program?

The FA Identified program is supported by a team of experts at Prevention Genetics who can help at every step, from placing the order to understanding results. If you have questions about what your genetic results mean, your healthcare provider can also connect you with additional genetic counseling resources.

Who qualifies for FA Identified Friedreich Ataxia genetic testing?

Patients may qualify for FA Identified if they meet the program's eligibility criteria:

  • Must be 16 years of age or older.
  • Must reside in the United States or Puerto Rico.
  • Must have a suspected or clinical diagnosis of Friedreich Ataxia (FA).
  • Testing must be ordered by a qualified health care provider.

Test details

  • ConditionFriedreich Ataxia (FA)
  • Test typeNGS
  • Test code20060
  • Genes / markers
    1
  • Key genes / markersFXN
  • SpecimenWhole blood•Saliva•Buccal swab
  • Turnaround time2-3 Weeks
  • LabPrevention Genetics
  • Program regionUnited States, Puerto Rico

Next steps

Share this information with your healthcare provider or genetic specialist. They can help determine whether this test and program are appropriate for you.

Or ask your doctor to search for this test by name at Prevention Genetics.

Questions to ask your doctor about Friedreich Ataxia Genetic Evaluation

  1. Do you think this test is appropriate for me based on my symptoms and history?
  2. How could the results of this test change my diagnosis or treatment plan?
  3. What are the potential limitations of this test that I should understand?
  4. Should any of my family members also be tested based on my results?
  5. How will we follow up after the results are available?

Notes

See an issue with this program?

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