Who Should Consider Genomic Testing?

People with a personal or family history of cancer. Genomic testing can help identify gene mutations that increase your risk of developing certain types of cancer, such as breast cancer, ovarian cancer, prostate cancer, and colon cancer. This information can help you make decisions about your health care, such as whether to have regular screenings or take preventive medications.

People with a rare disease or disorder. Genomic testing can help identify the genetic cause of a rare disease or disorder, such as cystic fibrosis, sickle cell anemia, or Gaucher disease. This information can help you get the appropriate treatment and support.

People who are pregnant or planning to become pregnant. Genomic testing can help identify genetic conditions that could affect your pregnancy or the health of your child. This information can help you make decisions about your prenatal care and delivery plan.

People who are interested in learning more about their ancestry or genetic traits. Genomic testing can provide information about your genetic heritage and ancestry, as well as your risk of developing certain genetic conditions. This information can be interesting and informative, and it can help you make informed decisions about your health care.

It's important to talk to your doctor or genetic counselor to see if genomic testing is right for you. They can help you understand the benefits and risks of testing and make sure you're getting the most accurate and relevant results.