Compare this test’s laboratory options
BRCA Panel Plus
Quest Diagnostics1 test optionFrom $7,230.01
BRCA Panel Plus
Quest DiagnosticsWhat this laboratory test evaluates
BRCA Panel Plus
This test is crucial for understanding hereditary breast cancer. While 5-10% of breast cancer cases are inherited, genes known as BRCA1 and BRCA2 are responsible for 15-20% of these hereditary cases. Additionally, five other genes (CDH1, PALB2, PTEN, STK11, and TP53) are analyzed because they can explain another 3% to 4.5% of hereditary breast cancers. Knowing if these genes have any changes (mutations) can help assess the risk of developing breast cancer.
Who should consider this test?This test may be recommended for individuals with a family history of breast cancer, providing valuable information for managing their health.
What type of sample is required for this test?5 mL of whole blood collected in an EDTA (lavender-top) or ACD (yellow-top) tube.
A simple blood draw is needed.
Test Resources
https://education.questdiagnostics.com/faq/FAQ230
Additional test information
This test may be recommended for individuals with a family history of breast cancer, providing valuable information for managing their health.
Collection and processing
- Sample type: Whole blood
- Fasting: No
- Estimated laboratory processing: Results should be available in 2 – 5 business days after the sample is collected
How Sunridge uses laboratory information
Sunridge considers the medical question, symptoms, history, medications, prior results, and whether the finding could change care before recommending testing. A laboratory result is not interpreted in isolation and does not establish a diagnosis by itself.
Before requesting this test
Availability, collection requirements, eligibility, and processing estimates can change. Sunridge reviews each request and, when appropriate, creates the order through Fullscript. Follow the current instructions supplied with the approved order.
About this test
BRCA Panel Plus
This test is crucial for understanding hereditary breast cancer. While 5-10% of breast cancer cases are inherited, genes known as BRCA1 and BRCA2 are responsible for 15-20% of these hereditary cases. Additionally, five other genes (CDH1, PALB2, PTEN, STK11, and TP53) are analyzed because they can explain another 3% to 4.5% of hereditary breast cancers. Knowing if these genes have any changes (mutations) can help assess the risk of developing breast cancer.
Who should consider this test?This test may be recommended for individuals with a family history of breast cancer, providing valuable information for managing their health.
What type of sample is required for this test?5 mL of whole blood collected in an EDTA (lavender-top) or ACD (yellow-top) tube.
A simple blood draw is needed.
Test Resources
https://education.questdiagnostics.com/faq/FAQ230
Additional details
This test may be recommended for individuals with a family history of breast cancer, providing valuable information for managing their health.
Highlighted health areas
- Genetics
Biomarkers and report focus
The exact analytes and report format can change. Confirm the current contents in the Fullscript order before payment.
- Brca1
- Brca2
- Cdh1
- Palb2
- Pten
- Stk11
- Tp53