This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v2.1.0: STU 2) based on FHIR R4. This is the current published version. For a full list of available versions, see the Directory of published versions
Official URL: http://hl7.org/fhir/us/mcode/ValueSet/mcode-clinvar-vs | Version: 2.1.0 | |||
Active as of 2023-03-21 | Computable Name: ClinVarVS |
Value set of human genomic variants, drawn from ClinVar. The codes in this value set refer to the ClinVar Variation ID, or the identifier for the variant or set of variants that were interpreted. Source: NCBI ClinVar Data Dictionary
References
http://www.ncbi.nlm.nih.gov/clinvar
No Expansion for this valueset (Unknown Code System)
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 |