Genomics Reporting Implementation Guide
3.0.1-SNAPSHOT - Ballot International flag

Genomics Reporting Implementation Guide, published by HL7 International / Clinical Genomics. This guide is not an authorized publication; it is the continuous build for version 3.0.1-SNAPSHOT built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/genomics-reporting/ and changes regularly. See the Directory of published versions

CodeSystem: ClinVar Evidence Level Example Codes

Official URL: http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/clinvar-evidence-level-custom-cs Version: 3.0.1-SNAPSHOT
Active as of 2024-07-15 Computable Name: ClinVarEvidenceLevelCustomCS

ClinVar contains examples of evidence level concepts that are not conflated with clinical significance. These can be found on ClinVar https://www.ncbi.nlm.nih.gov/clinvar/docs/review_status/ . These examples are informational only, for copyright information contact the relevant source.

This Code system is referenced in the content logical definition of the following value sets:

Generated Narrative: CodeSystem clinvar-evidence-level-custom-cs

This case-sensitive code system http://hl7.org/fhir/uv/genomics-reporting/CodeSystem/clinvar-evidence-level-custom-cs defines the following codes:

CodeDisplayDefinition
4-star 4 star Supported by practice guideline
3-star 3 star Supported by expert panel review
2-star 2 star Supported by submission by multiple-submitters with documentation of criteria for assertion
1-star 1 star Single submitter providing interpretation and documentation of criteria for assertion
no-star no star submitted, no evidence