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.
Hereditary breast cancer refers to breast cancer that is caused by inherited genetic variants. These variants significantly increase the risk of developing breast cancer and can be passed from parents to their children.
Approximately 5-10% of all breast cancers are hereditary. The most common cause is an inherited variant in the BRCA1 or BRCA2 genes, but other high-risk genes include TP53 (Li-Fraumeni syndrome), PTEN (Cowden syndrome), and STK11 (Peutz-Jeghers syndrome), while moderate-risk genes include PALB2, and CDH1. The prevalence of BRCA1 and BRCA2 pathogenic variants in the general population is estimated at 1 in 100-200.