{
  "package" : "hl7.terminology.r5@6.3.0",
  "definition" : "ClinVar Variant ID",
  "system" : "http://terminology.hl7.org/CodeSystem/v2-0396",
  "property" : [ {
    "_uri" : "http://terminology.hl7.org/CodeSystem/utg-concept-properties#v2-concComment",
    "code" : "v2-concComment",
    "valueString" : "ClinVar processes submissions reporting variants found in patient samples, assertions made regarding their clinical significance, information about the submitter, and other supporting data. The alleles described in submissions are mapped to reference sequences, and reported according to the HGVS standard."
  }, {
    "_uri" : "http://terminology.hl7.org/CodeSystem/utg-concept-properties#status",
    "code" : "status",
    "valueCode" : "A"
  } ],
  "codesystem" : "cb8cdb18-a074-5e6c-a3b7-57416f28931c",
  "concept_id" : "dd40d725-b534-5589-bcd2-728d24932e98",
  "ancestors" : {
    "CLINVAR-V" : 0
  },
  "id" : "e43372a6-c040-4f0b-a23d-317b58e4b4ba",
  "code" : "CLINVAR-V",
  "display" : "ClinVar Variant ID",
  "version" : "4.1.0"
}