BRCA1/BRCA2 Comprehensive (Sequencing and Deletion/Duplication) Test
50+ booked in last 3 daysTest Overview
Test ordered in Individuals With Strong Family History of Breast or Ovarian Cancer (HBOC).
Frequently Asked Questions
The assay detect mutation and large deletion / duplication in BRCA1 and BRCA2 gene.
As suggested by doctor to test in Individuals With Strong Family History of Breast or Ovarian Cancer (HBOC).
Test ordered in Individuals With Strong Family History of Breast or Ovarian Cancer (HBOC). The assay detect mutation in BRCA1 and BRCA2 gene. Evaluation for patients with a personal or family history suggestive of hereditary breast and ovarian cancer (HBOC) syndrome. Establishing a diagnosis of HBOC syndrome allowing for targeted cancer surveillance based on associated risks. Identifying variants within genes known to be associated with increased risk for HBOC syndrome allowing for predictive testing of at-risk family members. Therapeutic eligibility including poly adenosine diphosphate-ribose polymerase (PARP) inhibitors in select cancer types.
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