Baldwin - GA

Fanconi Anemia Carrier Test - FA Carrier in Baldwin, GA

The Fanconi anemia carrier test is a genetic blood test that looks for two specific mutations in the FANCC gene associated with Fanconi anemia type C. Fanconi Anemia Carrier Test - FA Carrier testing in Baldwin, GA: order online, visit a patient service center near you, and review your results in a secure account.

Typical price

From $199

Results

1-3 business days

Preparation

See preparation notes below

The Fanconi anemia carrier test is a genetic blood test that looks for two specific mutations in the FANCC gene associated with Fanconi anemia type C. It can identify people who carry one copy of a mutation, known as carriers, as well as individuals who may be affected. The two mutations tested are IVS4+4A>T and 322delG. This test is often considered by people with a family history of the condition or by couples planning a pregnancy who want information about carrier status. Genetic counseling is recommended before and after testing so results can be explained in context.

• FANCC IVS4+4A>T mutation A specific change in the FANCC gene tested to identify carriers of and individuals affected by Fanconi anemia type C.
• FANCC 322delG mutation A specific deletion in the FANCC gene tested to identify carriers of and individuals affected by Fanconi anemia type C.

• People with a family history of Fanconi anemia or bone marrow failure
• Couples planning a pregnancy who want carrier information
• Individuals with a personal or family history suggesting a Fanconi anemia diagnosis
• People of ancestry in which one of the tested FANCC mutations is more common
• Anyone whose healthcare provider recommends carrier screening based on family history

• No fasting is required for this test
• A blood sample is collected, or sometimes a saliva sample, depending on the lab
• Genetic counseling is recommended before testing to review what the results can and cannot show
• Tell the lab about any prior genetic testing or family history information

A negative result means neither tested FANCC mutation was detected, which lowers the likelihood of being a carrier for those specific changes but does not rule out other mutations. Detecting one mutation may indicate carrier status, while detecting two may indicate that a person is affected, depending on the clinical context. Because genetic results carry implications for family members and family planning, they are interpreted with genetic counseling. Discuss your result with a healthcare provider or genetic counselor before drawing conclusions.

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