Since multigene panel testing (MGPT) for hereditary cancer syndromes became available in 2012, multiple laboratories have offered various MGPT options ranging in size and scope. Smaller panels consisting of “high-risk” genes are favored by some clinicians due to the availability of management guidelines, lower chance of an incidental finding, and lower variant of uncertain significance (VUS) rates; whereas larger panels are favored by others due to their comprehensive nature. Since 2012, utilization of MGPT has increased while single-syndrome testing has decreased across many physician specialties. This study aims to explore the utilization of breast cancer (BC)-specific and comprehensive cancer panels among clinicians of various specialties in breast cancer patients.