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Clinical Trial Summary

This is a genomic implementation project with ancillary studies to understand the impact on patients' health and well-being of returning genomic results to them and depositing those results in the medical record.


Clinical Trial Description

Study participant DNA samples will be sequenced for 109 genes of interest along with genotyping of select polymorphisms. Genetic tests will be performed in a Clinical Laboratory Improvement Amendments (CLIA) certified lab (Baylor Human Genome Sequencing Laboratory). Selected results (pathogenic/likely pathogenic) will be returned to participants by a genetic counselor and deposited into the Electronic Health Record (EHR). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03640234
Study type Observational
Source Mayo Clinic
Contact
Status Completed
Phase
Start date February 25, 2016
Completion date September 1, 2022

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