For clinics
Clear information. A conversation about what comes next.
Polygenic scores are new to most clinicians, so we explain clearly how to read them.
When a patient connects you
You can read their report, download a structured export of the underlying values, and write private notes. Notes are hidden if the patient ends the connection and deleted if they delete their account, so keep your patient records in your own system. Your access depends on their consent and ends when they end the connection.
Where a patient has consented, a report can also show a combined risk estimate that adds health and lifestyle data to genetics.
Your notes stay private unless you share them
You can share an individual note with the patient. They see the note as it was when you shared it, and your later edits stay with you.
Interpretation guidance
Guidance on what a score means, such as the difference between a percentile and an absolute risk, is reviewed by a named person on our team before it reaches you. Notes you write and share stay your own.
What is available today
Today
A member can download their report as a PDF and hand it to a clinician.
Clinician portal
A connected clinician can read the report, download a structured export and write private notes, with the patient’s consent. We are improving it with our founding clinics.
Coming soon
Ordering through a clinic, EHR integration and white-label versions. The API for provider records is developed, and we are seeking partners.
Reading a score
- Informational and Research Use Only, and not for clinical or medical decision-making.
- Scores are relative to a reference population, and calibration varies by ancestry.
- A high score is a reason to discuss screening, and a low score does not rule a condition out. Neither is a clinical finding.
