Scientists recruit 1,000 people to unlock secrets of surprise gene changes
NCT ID NCT03632239
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
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.
Disclaimer
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This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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The condition terms exactly as the trial's registrant entered them.
Contacts and locations
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Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States