Abstract:10617 Background: Identification of pathogenic germline variants (PGVs) is important in guiding treatment decisions, cancer screening and testing of family members. While genetic testing indications expand, barriers to testing still exist. Streamlined processes for genetic testing are needed. Our study assessed the feasibility of a novel approach in which patients with cancer underwent genetic testing first with genetic counseling after for only those with a PGV. Methods: This was an IRB approved study of pat… Show more
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