Typical user questions a genome RAG would answer

Representative questions:

"What does my BRCA1 variant mean for my cancer risk?"
"Is this variant pathogenic or uncertain?"
"What conditions are associated with the findings in my report?"
"What does VUS mean?"
"Which of my variants affect drug metabolism (pharmacogenomics)?"

Each maps to retrieving the relevant annotated variant + reference explanation and generating a grounded, cited, appropriately-hedged answer with a "discuss with your clinician/genetic counselor" boundary.