This page is part of the Genetic Reporting Implementation Guide (v1.1.0: STU 2 Ballot 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
<Observation xmlns="http://hl7.org/fhir">
<id value="Pgx-var-1019"/>
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<profile
value="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/variant"/>
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<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative</b></p><p></p><p><b>category</b>: <span title="Codes: {http://terminology.hl7.org/CodeSystem/observation-category laboratory}">Laboratory</span></p><p><b>code</b>: <span title="Codes: {http://loinc.org 69548-6}">Genetic variant assessment</span></p><p><b>subject</b>: <a href="Patient-CGPatientExample01.html">Generated Summary: Medical Record Number: m123 (USUAL); Adam B. Everyman ; gender: male; birthDate: 1951-01-20</a></p><p><b>effective</b>: 2020-01-01</p><p><b>value</b>: <span title="Codes: {http://loinc.org LA9633-4}">Present</span></p><p><b>method</b>: <span title="Codes: {http://loinc.org LA26398-0}">Sequencing</span></p><blockquote><p><b>component</b></p><p><b>code</b>: <span title="Codes: {http://loinc.org 81290-9}">Genomic DNA change (gHGVS)</span></p><p><b>value</b>: <span title="Codes: {http://varnomen.hgvs.org NC_000016.9:g.31096368C>T}">NC_000016.9:g.31096368C>T</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: <span title="Codes: {http://loinc.org 48002-0}">Genomic source class [Type]</span></p><p><b>value</b>: <span title="Codes: {http://loinc.org LA6683-2}">Germline</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: <span title="Codes: {http://loinc.org 53034-5}">Allelic state</span></p><p><b>value</b>: <span title="Codes: {http://loinc.org LA6706-1}">heterozygous</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: <span title="Codes: {http://loinc.org 48018-6}">Gene studied [ID]</span></p><p><b>value</b>: <span title="Codes: {http://www.genenames.org/geneId HGNC:23663}">VKORC1</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: <span title="Codes: {http://loinc.org 48019-4}">DNA Change Type</span></p><p><b>value</b>: <span title="Codes: {http://sequenceontology.org SO:1000002}">substitution</span></p></blockquote><blockquote><p><b>component</b></p><p><b>code</b>: <span title="Codes: {http://loinc.org 82121-5}">Allelic read depth</span></p><p><b>value</b>: >20</p></blockquote></div>
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<status value="final"/>
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<code value="laboratory"/>
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<system value="http://loinc.org"/>
<code value="69548-6"/>
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<reference value="Patient/CGPatientExample01"/>
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<effectiveDateTime value="2020-01-01"/>
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<coding>
<system value="http://loinc.org"/>
<code value="LA9633-4"/>
<display value="Present"/>
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<code value="LA26398-0"/>
<display value="Sequencing"/>
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<code value="LA6683-2"/>
<display value="Germline"/>
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<coding>
<system value="http://loinc.org"/>
<code value="53034-5"/>
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<coding>
<system value="http://loinc.org"/>
<code value="LA6706-1"/>
<display value="heterozygous"/>
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<coding>
<system value="http://loinc.org"/>
<code value="48018-6"/>
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<coding>
<system value="http://www.genenames.org/geneId"/>
<code value="HGNC:23663"/>
<display value="VKORC1"/>
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<coding>
<system value="http://loinc.org"/>
<code value="48019-4"/>
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<code value="SO:1000002"/>
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<coding>
<system value="http://loinc.org"/>
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