This page is part of the Genetic Reporting Implementation Guide (v2.0.0: 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
<DocumentReference xmlns="http://hl7.org/fhir">
<id value="VCFFile"/>
<meta>
<profile
value="http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/genomics-document-reference"/>
</meta>
<text>
<status value="generated"/>
<div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative</b></p><div style="display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%"><p style="margin-bottom: 0px">Resource "VCFFile" </p><p style="margin-bottom: 0px">Profile: <a href="StructureDefinition-genomics-document-reference.html">Genomics DocumentReference</a></p></div><p><b>status</b>: current</p><p><b>subject</b>: <a href="Patient-CGPatientExample01.html">Patient/CGPatientExample01</a> " EVERYMAN"</p><p><b>description</b>: ... details about how this VCF was generated ...</p><blockquote><p><b>content</b></p></blockquote><h3>Contexts</h3><table class="grid"><tr><td>-</td><td><b>Related</b></td></tr><tr><td>*</td><td><a href="DiagnosticReport-PGxGenomicsReportEMERGE.html">DiagnosticReport/PGxGenomicsReportEMERGE</a></td></tr></table></div>
</text>
<status value="current"/>
<subject>
<reference value="Patient/CGPatientExample01"/>
</subject>
<description value="... details about how this VCF was generated ..."/>
<content>
<attachment>
<url
value="http://ftp.1000genomes.ebi.ac.uk/vol1/ftp/release/20130502/ALL.chr1.phase3_shapeit2_mvncall_integrated_v5b.20130502.genotypes.vcf.gz"/>
</attachment>
</content>
<context>
<related>
<reference value="DiagnosticReport/PGxGenomicsReportEMERGE"/>
</related>
</context>
</DocumentReference>