Your records, labs, medications and your genome, together so your doctor sees the whole picture. Not just what’s wrong today, but what’s worth getting ahead of.
You’re being asked about four things:
Each is a separate choice. None of them affects the care you receive, and you can change your mind at any time.
Genetic results are protected from health insurance and employment discrimination by federal law (GINA), but not life or disability insurance. More about GINA
Each one is separate and independent. Your care never depends on any of them, and you can change any of these later. Open “Read the full wording” to see the exact consent language.
One tap sets all six. You can switch any of them off.
Lets your practice use GenSec to bring your records together.
Adds your genome to the picture. Off means no test is ordered.
Your clinical history over time, with identifying details removed.
Only applies if you’ve chosen genome testing above.
Means keeping your information linked to you rather than anonymous. We may reach out — we don’t promise to monitor your data on any schedule.
Taking part is always separate and voluntary.
Whatever you choose above, any data shared for research is de-identified first — details that could identify you (your name, date of birth, address, contact details and the like) are removed or replaced.
Check your details and your choices. You’ll sign the consent document itself in the next step.
Your choices are filled in already. You can still change any of them in the document before you sign. You’ll be asked for a code sent to your email.
Scroll to the end of the document — there is a second signature on the state addendum page.
Thank you. Your choices have been recorded.