Testing for at-risk family members
Genetic test results may have health implications not only for an individual, but for an entire family. If you receive a positive test result, family follow-up testing can help identify other family members at risk for the same genetic disease. Family members who test positive can work with their doctors to make a plan for prevention or early detection of disease.
If you tested positive for a disease-causing (pathogenic or likely pathogenic) variant, your family members have up to a 50% chance of having the same variant. If they also test positive, they may have an elevated risk of developing the disease and can look into options for prevention and early detection. If they test negative, their risk of developing the disease may be similar to the general population.
There are a few steps you can take:
– Talk to your doctor or our genetic counselors to determine which of your family members could be at risk.
– Provide your family members with a copy of your genetic test report. We know that discussing your health can be difficult, so we created template letters to family members to help begin the conversation.- Encourage your family members to discuss the option of genetic testing with their doctor or a genetic counselor.
If your family member has a disease-causing (pathogenic or likely pathogenic) variant, you may have up to a 50% chance of having the same variant. If you also test positive, you may have an elevated risk of developing the disease. With this knowledge, you can consider options for prevention and early detection. If you test negative, your risk of developing the disease may be similar to the general population.
There are a few steps you can take:
– Obtain a copy of your relative’s positive genetic test report.
If you would like your doctor to order genetic testing for you, bring this letter and your relative’s test report to your doctor’s appointment. Some doctors will order genetic testing directly, while others will refer you to a genetic.