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Read about different genes that are linked to hereditary cancer, their associated risks and guidelines for screening, preventing and treating cancers in people with inherited mutations in these genes.
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Hereditary Cancer and Genetic Testing

Hereditary Cancer Genes and Risk > By Gene Mutation > PALB2 > Cancer Risk

1
Overview
2
Cancer Risk
3
Risk Management
4
Cancer Treatment
5
Other Considerations

Cancer risk associated with an inherited mutation

If you have tested positive for a  mutation, we recommend that you consult with a genetics expert who can assess your personal and family history of cancer, and help you determine the best risk management plan.

Increased lifetime cancer risks associated with a  mutation:

  • Women who have a mutation in are at increased risk for breast cancer. The estimated lifetime risk is between 40 - 60 percent.
  • Women with a mutation have an increased risk for ovarian cancer. The estimated lifetime risk is between 3 - 5 percent.  
  • Men and women with a mutation are at increased risk for pancreatic cancer. The estimated lifetime risk is about 5 - 10 percent. 
  • There is unknown or insufficient evidence of risk for other cancers in people with a mutation. 

Graph of lifetime breast cancer risk in women with <button x-data class='glossary-tip tt-palb2' x-tooltip='<p>PALB2 is a gene found on chromosome 16.&nbsp;Mutations in PALB2&nbsp;increase the risk for&nbsp;female breast and pancreatic cancer,&nbsp;and possibly other cancers.</p> ' >PALB2</button> mutations   Graph of lifetime risk for pancreatic cancer for person with a <button x-data class='glossary-tip tt-palb2' x-tooltip='<p>PALB2 is a gene found on chromosome 16.&nbsp;Mutations in PALB2&nbsp;increase the risk for&nbsp;female breast and pancreatic cancer,&nbsp;and possibly other cancers.</p> ' >PALB2</button> mutation

find-support find-support

FORCE offers many peer support programs for people with inherited mutations. 

updated: 03/12/2022

related-resources related-resources

The following resources focus on mutations. 

updated: 03/16/2022

clinical-trials clinical-trials

NCT02665195: Registry Of MultiPlex Testing (PROMPT). PROMPT is an online research registry. The goal of PROMPT is to help researchers to better understand the risks that are linked to mutations in less well-studied genes. People with inherited mutations can enroll in PROMPT to help researchers learn more about cancer risks. 

updated: 02/05/2022

Last updated March 15, 2022