Screens for variants in Familial Adenomatous Polyposis genes.
Guidelines recommend testing to confirm the diagnosis of an inherited CRC syndrome in a patient with a personal history of disease in the following circumstances:
FAP Gene Panel
Used for investigation of FAP/MAP in patients with adenomatous polyposis where there is a familial risk of ≥10%.
APC, MUTYH
Massively Parallel Sequencing
4 weeks
73355 – conditions apply
$479 if not Medicare eligible
Cancer Genetics Request form preferred. Standard pathology request form accepted.
Blood x 2
6mL EDTA
2 x Bloods taken at 10 minute intervals. Pre test genetic counselling required. Patient to sign consent form prior to testing.