When a patient receives a cancer diagnosis or presents with features that point to a single hereditary cancer syndrome, single-gene analysis can pinpoint whether the disease is genetic in nature.
Identifies variants within genes known to be associated with increased risk for Birt-Hogg-Dube syndrome, allowing for predictive testing of at-risk family members.
Identifies genetic variants associated with increased risk for BAP1-tumor predisposition syndrome, allowing for predictive testing and appropriate screening of at-risk family members.