Genomics Reporting Implementation Guide
2.0.0 - trial-use

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

Example DiagnosticReport: PGxGenomicsReportEMERGE-withGrouping

emerge-seq-ngs-pnl (Genetics)

SubjectAdam B. Everyman male, DoB: 1951-01-20 ( Medical Record Number: m123 (USUAL))
When For2020-01-01 12:00:00-0500
Reported2020-01-01 12:00:00-0500

Report Details

CodeValue
Discrete variation analysis overall interpretationPositive
Group
Group
Group