10,000 french genomes to unlock better diagnoses
NCT ID NCT04183023
First seen Apr 01, 2026 · Last updated Jun 13, 2026 · Updated 10 times
Summary
This study aims to create a reference map of genetic variations found in the general French population. By analyzing DNA from 10,000 volunteers, researchers hope to better identify which genetic changes are likely to cause disease. This will help doctors filter out common, harmless variants when diagnosing patients with genetic conditions.
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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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Locations
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Inserm - UMR1078 GGB
Brest, France
Conditions
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