For more on Risk Assessment
at Fox Chase Cancer Center,
call 1-877-627-9684.
Learn More: Genetic Testing Information
- Our History
- What are Risk Factors
- Genetic Testing Information
- Progress through Research
Individuals interested in having genetic testing meet with a genetic counselor or risk assessment nurse to discuss their genetic risk of developing cancer as well as to help determine if their family could have a hereditary cancer syndrome. During a genetic counseling session, an individual’s personal and family history of cancer is reviewed. The genetic counselor or risk assessment nurse will determine if genetic testing is appropriate. If so, benefits, risks, and limitations of genetic testing will be discussed. Also reviewed is the psychosocial and emotional impact test results may have for you and your family.
If you decide to have testing, you will receive your genetic test results from your genetic counselor or risk assessment nurse. A nurse practitioner or physician is also present to review medical management and screening recommendations. A plan may be developed to help communicate results to your family members and medical professionals.
If you have any questions about genetic testing and whether or not it is right for you, please call us at 1-877-627-9684.
| Cancer/Syndrome | Gene |
Hereditary Breast and Ovarian Cancer |
BRCA1 & BRCA2 |
Lynch Syndrome or Hereditary Nonpolyposis Colon Cancer (HNPCC) |
MSH2, MLH1, MSH6 & PMS2 |
Familial Adenomatous Polyposis (FAP) |
APC |
Hereditary Prostate Cancer |
BRCA1 & BRCA2, others |
Hereditary Melanoma & Basal Cell Nevus Syndrome |
CDK4, CDKN2A, CMM & P16 |
Li Fraumeni Syndrome |
P53, CHEK2 |
Cowden Syndrome |
PTEN |
Multiple Endocrine Neoplasia, Type I |
MEN1 |
Multiple Endocrine Neoplasia, Type II, Medullary Thyroid Carcinoma |
RET |
von Hippel-Lindau Syndrome |
VHL |


Print this Page








