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 - JSON Representation
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{
"resourceType" : "ValueSet",
"id" : "mcode-clinvar-vs",
"text" : {
"status" : "generated",
"div" : "<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>"
},
"url" : "http://hl7.org/fhir/us/mcode/ValueSet/mcode-clinvar-vs",
"version" : "2.1.0",
"name" : "ClinVarVS",
"title" : "ClinVar Value Set",
"status" : "active",
"experimental" : false,
"date" : "2023-03-21T04:54:56+11:00",
"publisher" : "HL7 International Clinical Interoperability Council",
"contact" : [
{
"name" : "HL7 International Clinical Interoperability Council",
"telecom" : [
{
"system" : "url",
"value" : "http://www.hl7.org/Special/committees/cic"
},
{
"system" : "email",
"value" : "ciclist@lists.HL7.org"
}
]
}
],
"description" : "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" : "urn:iso:std:iso:3166",
"code" : "US",
"display" : "United States of America"
}
]
}
],
"compose" : {
"include" : [
{
"system" : "http://www.ncbi.nlm.nih.gov/clinvar"
}
]
}
}