

The BRCA1 and BRCA2 test is a genetic screening designed to detect mutations (abnormal changes) in two genes: BRCA1 and BRCA2. These genes help repair DNA damage and maintain the stability of your genetic material.
When mutations occur in either gene, the body’s ability to fix damaged cells is compromised—leading to a significantly higher risk of developing several types of cancer, especially:
Breast cancer
Ovarian cancer
Prostate cancer (in men)
Pancreatic cancer
Doctors often recommend BRCA testing for individuals at increased genetic risk, particularly in the following situations:
Family history of breast or ovarian cancer at a young age (before age 50)
Male relatives diagnosed with breast cancer
Multiple types of cancer present in the family
A personal history of cancer in both breasts or both ovaries
Belonging to populations with higher mutation rates (e.g., Ashkenazi Jewish descent)
A sample of blood or saliva is collected, depending on the lab.
The sample is sent to a specialized genetic testing laboratory.
No fasting or special preparation is needed.
Results are typically available within 2 to 4 weeks.
BRCA1/BRCA2 test results are usually classified into three categories:
Result | Interpretation |
---|---|
Positive | A harmful mutation is present, significantly increasing your cancer risk. |
Negative | No known harmful mutations were found, though moderate risk may remain if there's a family history. |
VUS (Variant of Uncertain Significance) | A genetic change was detected, but its impact is not yet clear and requires further evaluation. |
A positive BRCA result does not mean you have cancer—but it does indicate a higher-than-average lifetime risk. For example:
The lifetime risk of breast cancer can rise to 70%.
The risk of ovarian cancer can reach up to 44%, especially with BRCA1 mutations.
However, knowing this risk gives you the power to act early and potentially prevent cancer.
Depending on your risk level and doctor’s guidance, the next steps may include:
Frequent screenings (e.g., breast MRI and ultrasounds)
Preventive medications (such as Tamoxifen)
Preventive surgery (e.g., mastectomy or oophorectomy in high-risk cases)
Genetic counseling for family members
Although BRCA mutations are more common in women, men can also benefit from BRCA testing, especially if:
They have a strong family history of cancer
They have had prostate or pancreatic cancer
They want to understand the risk of passing the mutation to their children
Women who carry a BRCA mutation can use this genetic information for reproductive planning, including:
Preimplantation genetic diagnosis (PGD) during IVF to avoid passing on the mutation
Regular screening during and after pregnancy
Consulting with a gynecologic oncologist for personalized risk management
BRCA testing is one of the most accurate genetic tests, with >99% sensitivity for known mutations. However, interpretation always requires a qualified healthcare professional, as results may have different implications based on personal and family history.
Do I need the test if I have no symptoms?
Yes. BRCA testing is mainly for preventive purposes, especially if there's a family history.
Is BRCA testing expensive?
It can be costly in some countries, but many healthcare systems and insurance plans offer coverage or financial support.
Can I take the test at any time?
Yes, as long as you’re not currently dealing with a serious illness that may interfere with the test.
Can my result change over time?
No. The genetic result is permanent, but the interpretation might evolve with ongoing research.
The BRCA1 and BRCA2 test is a powerful genetic screening tool that plays a critical role in early cancer prevention, particularly for breast and ovarian cancer.
Early testing = better preparation = wider treatment and prevention options.
If you or a family member has a history of cancer, don’t hesitate to speak with your doctor about taking the BRCA test—it could save your life.