0.2.0 - ci-build

GO_FHIR - Local Development build (v0.2.0) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions

ValueSet: GenomOncology Variant Significance

Official URL: http://fhir.genomoncology.io/ValueSet/variant-significance-valueset Version: 0.2.0
Active as of 2026-10-08 Computable Name: VariantSignificanceValueSet

Possible values for Variant Significance

References

Logical Definition (CLD)

 

Expansion

Expansion performed internally based on codesystem GenomOncology Variant Significance v0.2.0 (CodeSystem)

This value set contains 5 concepts

SystemCodeDisplay (en)JSONXML
http://fhir.genomoncology.io/CodeSystem/variant-significance-codesystem  oncogenicOncogenic
http://fhir.genomoncology.io/CodeSystem/variant-significance-codesystem  likely_oncogenicLikely Oncogenic
http://fhir.genomoncology.io/CodeSystem/variant-significance-codesystem  vusVUS
http://fhir.genomoncology.io/CodeSystem/variant-significance-codesystem  likely_benignLikely Benign
http://fhir.genomoncology.io/CodeSystem/variant-significance-codesystem  benignBenign

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code