This page is part of the HL7 FHIR Implementation Guide: minimal Common Oncology Data Elements (mCODE) Release 1 - US Realm | STU1 (v1.0.0: STU 1) based on FHIR R4. The current version which supercedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions

ClinVar Value Set

Summary

Defining URL:	http://hl7.org/fhir/us/mcode/ValueSet/mcode-clinvar-vs
Version:	1.0.0
Name:	ClinVarVS
Status:	Active
Title:	ClinVar Value Set
Definition:	Value set of human genetic 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
Publisher:	HL7 International Clinical Interoperability Council
Source Resource:	XML / JSON / Turtle

References

• Cancer Genetic Variant

Content Logical Definition

Definition

 

Expansion

No Expansion for this valueset (not supported by Publication Tooling)

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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
Source	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