Export reports as PDFs first
Clinicians expect PDF attachments or printed documents, not login credentials to a genomics portal. Export the relevant reports as PDFs before your appointment.
If you have many reports, share only those related to the visit's purpose. A cardiologist does not need your carrier screening panel; a reproductive specialist does.
Prepare a one-page summary
Lead with a brief summary: why you were tested, the test date, and the key findings you want to discuss. You can write this yourself or use an AI assistant to draft it from your PDFs.
Highlight pathogenic and likely pathogenic variants first. List VUS findings separately with a note that they may change classification.
Delivery methods that work
Patient portals: if your doctor's office has a secure messaging system, upload PDFs there.
Email: only if your clinic accepts it and you are comfortable with the security level. Consider password-protecting the PDF or using encrypted email.
In person: bring printed copies or a USB drive. This avoids any transfer privacy concerns entirely.
What to tell your doctor
Mention the testing company (Dante Labs), the test type (whole genome, exome, panel), and the date. Note if results have been updated or reclassified since the original report.
Ask specifically: "Do any of these findings change my care plan, screening schedule, or medication choices?"
Genetic counselor referral
For complex results (multiple VUS findings, unexpected pathogenic variants, or reproductive implications), ask for a referral to a genetic counselor. They specialize in interpreting and explaining genomic data.
Bring your full PDF archive to the counseling session. Counselors can work through large report libraries quickly.
Need help?
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