BRCA2 Mutation Status (Genetic Test for Inherited Cancer Risk)
This test checks for changes (mutations) in the BRCA2 gene, which may increase your risk of certain cancers, including breast and ovarian cancer. It’s often done if you have a family history of these cancers or if other genetic testing is recommended by your healthcare provider.
["Knowing your BRCA2 mutation status can help guide cancer prevention, screening, and treatment options."]
Key facts at a glance
- LOINC
- 96974-1
- Short code
- PALB2 Del+Dup Bld/T
- Synonyms
- PALB2 Del+Dup Bld/T
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- molgen
- Specimen volume
- 3 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 4–24 hours
- Order
- routine
Why This Test Might Be Ordered
Your doctor may suggest this test if you have a strong family history of breast, ovarian, prostate, or pancreatic cancer. It could also be recommended if you’ve been diagnosed with certain cancers at a younger age or if you’ve had multiple cancers in different areas of the body. Some genetic counseling services also perform this test for people with Ashkenazi Jewish ancestry, as certain mutations are more common in this group.
What to Expect Before the Test
You’ll need a blood sample drawn from a vein in your arm, similar to other blood tests. No special preparation is usually required, but your doctor might ask you to avoid certain medications or foods for a short time if instructed. The process is quick and typically causes only mild discomfort.
What the Test Results Mean
Results can be one of several types: negative (no mutation found), positive (mutation detected), or variant of uncertain significance (VUS), which means the mutation’s impact is unclear. A positive result means you may have a higher risk of certain cancers and could benefit from closer monitoring or preventive measures.
How This Test Affects Your Care
If you have a BRCA2 mutation, your doctor may recommend more frequent cancer screenings, such as mammograms, MRI scans, or ovarian ultrasounds. They might also suggest preventive surgeries like mastectomies or oophorectomies, depending on your personal and family history. Genetic counseling can help you understand your risks and make informed decisions about your health.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
BRCA2 Gene Mutation
Frequently asked questions
What does a BRCA2 mutation mean for my health?
How is this test different from other cancer screenings?
Can I get this test if I don’t have a family history of cancer?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy