Genomic Secondary Findings

Cross-source consensus on Genomic Secondary Findings from 1 sources and 5 claims.

1 sources · 5 claims

Evidence quality

Secondary findings are genomic variants unrelated to the original reason for testing but may indicate hereditary health risks. — Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study
The protocol uses secondary findings to refer to both secondary and incidental findings unless a specific analysis separates them. — Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study
The American College of Medical Genetics and Genomics recommends actively seeking and returning certain actionable secondary findings with prior consent. — Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study
The study focuses especially on pediatric settings because evidence and management guidance are limited there. — Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study
Canadian and European guidance is more cautious about returning secondary findings until stronger evidence exists. — Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study