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
: ClinVar Value Set - XML Representation
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<ValueSet xmlns="http://hl7.org/fhir">
<id value="mcode-clinvar-vs"/>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><ul><li>Include all codes defined in <a href="http://www.ncbi.nlm.nih.gov/clinvar"><code>http://www.ncbi.nlm.nih.gov/clinvar</code></a></li></ul></div>
</text>
<url value="http://hl7.org/fhir/us/mcode/ValueSet/mcode-clinvar-vs"/>
<version value="2.1.0"/>
<name value="ClinVarVS"/>
<title value="ClinVar Value Set"/>
<status value="active"/>
<experimental value="false"/>
<date value="2023-03-21T04:54:56+11:00"/>
<publisher value="HL7 International Clinical Interoperability Council"/>
<contact>
<name value="HL7 International Clinical Interoperability Council"/>
<telecom>
<system value="url"/>
<value value="http://www.hl7.org/Special/committees/cic"/>
</telecom>
<telecom>
<system value="email"/>
<value value="ciclist@lists.HL7.org"/>
</telecom>
</contact>
<description
value="Value set of human genomic variants, drawn from [ClinVar](https://www.ncbi.nlm.nih.gov/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](https://www.ncbi.nlm.nih.gov/projects/clinvar/ClinVarDataDictionary.pdf)"/>
<jurisdiction>
<coding>
<system value="urn:iso:std:iso:3166"/>
<code value="US"/>
<display value="United States of America"/>
</coding>
</jurisdiction>
<compose>
<include>
<system value="http://www.ncbi.nlm.nih.gov/clinvar"/>
</include>
</compose>
</ValueSet>