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)