Whole exome sequencing (WES) with in silico gene panel analysis.
Clinical Report (Download a sample report here)
~3-6 Weeks*
For detailed information about the sample requirements, please consult our clinical sample requirements page.
This is a subpanel based on our Hereditary Breast Cancer Panel.
This panel includes only BRCA1 and BRCA2 genes. BRCA1- and BRCA2-associated hereditary breast and ovarian cancer (HBOC) is characterized by an increased risk for female and male breast cancer (primarily BRCA2) , ovarian cancer (including fallopian tube and primary peritoneal cancers), and to a lesser extent other cancers such as prostate cancer, pancreatic cancer, and melanoma primarily in individuals with a BRCA2 pathogenic variant.
The prevalence of BRCA1 and BRCA2 pathogenic variants in the general population is estimated at 1 in 100-200.BRCA1- and BRCA2-associated HBOC is inherited in an autosomal dominant manner. The vast majority of individuals with a BRCA1 or BRCA2 pathogenic variant inherit it from a parent. However, because the penetrance of breast, ovarian, and other cancers associated with pathogenic variants in BRCA1 and BRCA2 is less than 100%, not all individuals with a BRCA1 or BRCA2 pathogenic variant have a parent affected with cancer.