Panel for genetic mutations linked to familial adenomatous polyposis.
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/MAP 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 patient not Medicare eligible.
Cancer Genetics request form preferred. Standard business unit form accepted.
Blood x 2
2 x 6mL EDTA tube
2 x Bloods taken at 10 minute intervals. Pre-test genetic counselling required.