Genetic tests look for changes in DNA that are associated with a high risk of inherited cancer. Testing helps inform individuals of cancer risk, including: breast, ovarian, colon, uterine and melanoma. Genetic counseling is performed before testing to develop a plan of action, which may include surgery, preventative therapies and frequent screenings.
Candidates may have:
Personal or family history of cancer
Family history of cancer diagnosed at a young age
Multiple family members with the same type of cancer
Family member with more than one cancer diagnosis
Family member with a rare type of cancer
Family history of a genetic alteration associated with a hereditary cancer syndrome
Genetic tests available:
BRCA1 (breast, ovarian, prostate)
BRCA2 (breast, ovarian, prostate, pancreatic)
MSH2, MLH1, MSH6 (colon, uterine, ovarian)
APC (colon with multiple polyps)
CDKN2, CDK4 (melanoma, pancreatic)
P53 (breast, bone, brain, leukemia)
RBI (retinoblastoma)
RET (medullary thyroid, parathyroid, pheochromocytoma)