Scientists recruit 1,000 people to unlock secrets of surprise gene changes
NCT ID NCT03632239
First seen Jun 24, 2026 · Last updated Aug 14, 2026 · Updated 4 times
Summary
This study enrolls 1,000 people who already have genetic sequencing data and may have unexpected gene variants. Researchers will collect health information, family history, and samples to see how these variants affect traits and health. The goal is to build a resource for scientists to learn more about genetic diseases and possible treatments.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this could help researchers better understand how certain genetic variants affect health, potentially pointing toward new treatments for genetic diseases.
- What could go wrong
- This is an observational study, not a treatment trial. It collects data but does not test any therapy, so direct benefits to participants are unlikely.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for HARBORING OF UNEXPECTED GENETIC VARIANT are added.
By submitting, you agree to our Terms of use
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States