This code system http://hl7.org/fhir/secondary-finding defines the following codes:

Code Display Definition
acmg-version1 ACMG Version 1 First release (2013): ACMG Recommendations for Reporting of Incidental Findings in Clinical Exome and Genome Sequencing. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727274/
acmg-version2 ACMG Version 2 Second release (2016): Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. https://www.ncbi.nlm.nih.gov/pubmed/27854360
<status value="draft"/> <experimental value="false"/> <date value="2025-09-13T16:38:45-04:00"/> <publisher value="Orders and Observations"/> <contact> <name value="Orders and Observations"/> <telecom> <system value="url"/> <value value="http://www.hl7.org/Special/committees/orders"/> </telecom> </contact> <description value="Codes to denote a guideline or policy statement.when a genetic test result is being shared as a secondary finding."/> <jurisdiction> <coding> <system value="http://unstats.un.org/unsd/methods/m49/m49.htm"/> <code value="001"/> <display value="World"/> </coding> </jurisdiction> <caseSensitive value="true"/> <valueSet value="http://hl7.org/fhir/ValueSet/secondary-finding|5.2.0"/> <content value="complete"/> <concept> <code value="acmg-version1"/> <display value="ACMG Version 1"/> <definition value="First release (2013): ACMG Recommendations for Reporting of Incidental Findings in Clinical Exome and Genome Sequencing. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727274/"/> </concept> <concept> <code value="acmg-version2"/> <display value="ACMG Version 2"/> <definition value="Second release (2016): Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. https://www.ncbi.nlm.nih.gov/pubmed/27854360"/> </concept> </CodeSystem>