Who could benefit from having a BRCA1/2 test?
You may consider testing :
If you or a close family member has a history of:
- Breast cancer before age 50
- Triple-negative breast cancer
- Ovarian, fallopian tube, or peritoneal cancer
- Multiple separate breast cancer diagnoses
- Male breast cancer
- Ashkenazi Jewish ancestry with breast cancer
- Several cases of breast and/or prostate cancer in the family
- A known BRCA1 or BRCA2 mutation in the family
Or if you have breast cancer currently and need to know BRCA1/2 status to guide therapy decisions
What are the BRCA1 and BRCA2 genes?
BRCA1 and BRCA2 are genes that help protect your cells from becoming cancerous.
When a change (mutation) is present in one of these genes, it can increase your chance of developing breast, ovarian, and other cancers. Knowing your genetic status empowers you to make informed, proactive decisions for your long-term health.
Benefits of the BRCA 1/2 Test
Fast, reliable turnaround time
Clinically validated testing
Trusted experience in hereditary cancer screening
How does the BRCA 1/2 test work?
Step 1
Complete form (includes sending us your prescription)
Choose one or more genetic tests from our online store. Receive your kit within 2 to 3 business days.
Step 2
Receive an e-mail with link to order your test online
Receive your kit within 3 to 5 business days.
Step 3
Collect your cheek swab sample
Follow the instructions in the kit, then send your saliva sample using the prepaid return envelope.
Step 4
Receive your report
Your results will be available within 4 weeks after we receive your sample.
Reliability. Safety. Trust.
All analyses are performed in our certified laboratory, following rigorous protocols to ensure the quality of results. The confidentiality and security of your health are ensured at every step of the process.
No. A positive (pathogenic) result for a gene like BRCA1 or BRCA2 means you have a genetic predisposition, which is a higher-than-average risk of developing certain cancers (e.g., breast, ovarian, prostate). However:
It is not a diagnosis: many people with a mutation will never develop cancer.
A positive result mainly helps guide preventive measures, such as more frequent screening, preventive medications, or surgical interventions if appropriate.
a) Positive result (pathogenic variant)
This means a genetic change known to increase the risk of certain cancers has been found. You can discuss preventive measures, enhanced monitoring, and the potential impactfor your familymembers.
b) Negative result
No mutation associated with increased risk was detected. This does not mean there is no risk of cancer, only that no known hereditary predisposition was identified.
c) Uncertain result (VUS variant of unknown significance)
A genetic change was observed, but its impact on health is not yet clearly established. In this case, no major clinical changes are recommended. Your medical team will continue to monitor you based on your personal and family history, and the variant may be reclassified as scientific knowledge advances.
Coverage for genetic tests depends on your private insurance and plan. We recommend contacting your insurance provider for more information about your coverage. You can obtain a quote for your genetic test at checkout to submit to your insurance company.
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