Test ID: FANCA
Fanconi Anemia C Mutation Analysis, IVS4(+4)A->T and 322delG
Secondary ID 
A test code used for billing and in test definitions created prior to November 2011
85318
Useful For Suggests clinical disorders or settings where the test may be helpful
Carrier testing for individuals of Ashkenazi Jewish ancestry
Prenatal diagnosis for at-risk pregnancies
Confirmation of clinical diagnosis in individuals of Ashkenazi Jewish Ancestry
Reflex Tests Lists test(s) that may or may not be performed, at an additional charge, depending on the result and interpretation of the initial test(s)
| Test ID | Secondary ID | Reporting Name | Available Separately | Always Performed |
|---|---|---|---|---|
| FBC | 80333 | Fibroblast Culture for Genetic Test | Yes | No |
| AFC | 80334 | Amniotic Fluid Culture/Genetic Test | Yes | No |
Testing Algorithm Delineates situation(s) when tests are added to the initial order. This includes reflex and additional tests.
Note: This testing algorithm only applies to prenatal testing.
If amniotic fluid (non-confluent cultured cells) is received, amniotic fluid culture/genetic test will be added and charged separately. If chorionic villus specimen (non-confluent cultured cells) is received, fibroblast culture for genetic test will be added and charged separately.
Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test
Method Name A short description of the method used to perform the test
FANCA/85318: Polymerase Chain Reaction (PCR) with Luminex Technology
FBC/80333, AFC/80334: Cell Culture
(PCR is utilized pursuant to a license agreement with Roche Molecular Systems, Inc.)
Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name
Fanconi Anemia, Mutation Analysis
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