This page is part of the Genetic Reporting Implementation Guide (v3.0.0: STU3) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version. For a full list of available versions, see the Directory of published versions
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"id" : "PGXGenomicStudyAnalysis",
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🔗 "http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomic-study-analysis"
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"div" : "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p class=\"res-header-id\"><b>Generated Narrative: Procedure PGXGenomicStudyAnalysis</b></p><a name=\"PGXGenomicStudyAnalysis\"> </a><a name=\"hcPGXGenomicStudyAnalysis\"> </a><a name=\"PGXGenomicStudyAnalysis-en-US\"> </a><p><b>Genomic Study Analysis Genome Build</b>: <span title=\"Codes:{http://loinc.org LA26806-2}\">GRCh38</span></p><blockquote><p><b>Genomic Study Analysis Metrics</b></p><ul><li>sequencing-coverage: 100</li></ul></blockquote><blockquote><p><b>Genomic Study Analysis Regions</b></p><ul><li>description: protein-coding and exon-splicing regions</li><li>studied: <span title=\"Codes:{http://www.genenames.org HGNC:2621}\">CYP2C19</span></li><li>studied: <span title=\"Codes:{http://www.genenames.org HGNC:2623}\">CYP2C9</span></li><li>studied: <span title=\"Codes:{http://www.genenames.org HGNC:23663}\">VKORC1</span></li></ul></blockquote><p><b>status</b>: Completed</p><p><b>category</b>: <span title=\"Codes:{http://terminology.hl7.org/CodeSystem/observation-category laboratory}\">Laboratory</span></p><p><b>subject</b>: <a href=\"Patient-CGPatientExample01.html\">Adam B. Everyman Male, DoB: 1951-01-20 ( Medical Record Number: m123\u00a0(use:\u00a0usual,\u00a0))</a></p><p><b>performed</b>: 2021-01-01 01:01:10-0600</p></div>"
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🔗 "reference" : "Patient/CGPatientExample01"
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