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Everything in one place

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:

  • Using your information to support your care
  • Adding genome testing
  • Helping research — with universities, hospitals and life-science companies
  • Letting us contact you if something could help your health

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

Your choices

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.

Accept all

One tap sets all six. You can switch any of them off.

Use my information to support my care

Lets your practice use GenSec to bring your records together.

Read the full wording
4a. Use of GenSec for your clinical care — please select one:
☐ I authorize my physician practice to use GenSec to support my clinical care, including (if I elect it below) the use of my genetic test results.
☐ I do not authorize use of GenSec for my clinical care at this time.

Include genome testing

Adds your genome to the picture. Off means no test is ordered.

Read the full wording
4b. Genetic testing — please select one:
☐ I authorize genetic testing as described above.
☐ I do not authorize genetic testing at this time. I understand I may change my mind in the future.

Use my de-identified health record for research

Your clinical history over time, with identifying details removed.

Read the full wording
10. Your Part B election
Clinical data (medical history, labs, imaging, treatments, outcomes):
☐ I authorize GenSec to include my de-identified clinical data in research datasets that may be shared with the partners listed in Section 7, including paid partnerships, as described in Sections 5–9.
☐ I do not authorize this use of my clinical data.

Use my de-identified genome for research

Only applies if you’ve chosen genome testing above.

Read the full wording
10. Your Part B election
Genetic data (if you have elected genetic testing in Part A):
☐ I authorize GenSec to include my de-identified genetic data in research datasets as described in Sections 5–9.
☐ I do not authorize this use of my genetic data.

Contact me if something could help my health

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.

Read the full wording
Being told about new findings relevant to your own health (optional)
Genomic science keeps advancing. Because GenSec holds your genome alongside your clinical record, information already collected can sometimes be re-examined as scientific understanding improves. If something emerges that may be relevant to your own health, GenSec or your physician practice may contact you or your practice so it can be reviewed with you.

To make this possible, GenSec needs to keep your information linked to you rather than only in de-identified form. If you decline this option, GenSec will not retain your information in identifiable form for this purpose beyond what your clinical care requires.

Important limits. GenSec may contact you but is under no obligation to do so. GenSec does not undertake to review, re-analyse, reinterpret, or monitor your information on any schedule, and you should not rely on GenSec to do so. Any new information would be reviewed with your physician, who remains responsible for your clinical care. Declining this option does not affect your care.

☐ I agree to be contacted if a re-examination of my information suggests something that may be relevant to my own health, and I authorize GenSec to retain my information in identifiable form for this purpose.
☐ I do not agree to this. I understand I may change my decision in the future.

Contact me about studies I may be eligible for

Taking part is always separate and voluntary.

Read the full wording
Being contacted about research opportunities (optional)
If your information suggests you may be eligible for a research study, clinical trial, or registry, GenSec or your physician practice may wish to contact you about it. Being contacted is not a guarantee of eligibility or benefit, and any actual participation would require its own separate consent.

☐ I agree to be contacted about research opportunities that may be relevant to me.
☐ I do not agree to be contacted about research opportunities.
🔒

Your identity stays protected

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.

Review & sign

Ready to sign

Check your details and your choices. You’ll sign the consent document itself in the next step.

We send your signing link and a one-time code here.
Each state adds its own addendum, which forms part of the document you sign.
Sign

Sign your consent

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.

All done

You’re all set.

Thank you. Your choices have been recorded.

  • 1
    Your clinician arranges your full-genome test and reviews results with you.
  • 2
    Your results appear in your GenSec Health record, alongside your history.
  • 3
    You can change any choice at any time — just tell your clinician.

· Questions? Call us at +1 (813) 515-0100.