Genomics Reporting Implementation Guide
3.0.0-ballot - Ballot International flag

This page is part of the Genetic Reporting Implementation Guide (v3.0.0-ballot: STU 3 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. The current version which supersedes this version is 2.0.0. For a full list of available versions, see the Directory of published versions

Example DiagnosticReport: PGxGenomicReportEMERGE

Genetic analysis report (Genetics)

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

Report Details

CodeValueNoteWhen For
Discrete variation analysis overall interpretationPositive2019-04-01
Therapeutic Implication2019-04-01
Therapeutic Implication2019-04-01
Therapeutic Implication2019-04-01
Therapeutic Implication2019-04-01
Therapeutic Implication2019-04-01
Therapeutic Implication2019-04-01
Genotype display nameCYP2C19*2/*22019-04-01
Genotype display nameVKORC1 rs9923231 C/T2019-04-01
Genotype display nameCYP2C9*1/*12019-04-01
Genetic variant assessmentPresent2020-01-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresent2019-04-01
Genetic variant assessmentPresentThis variant was confirmed with SANGER sequencing2019-04-01
Genetic variant assessmentPresentThis variant was confirmed with SANGER sequencing2019-04-01
Genetic variant assessmentPresentThis variant was confirmed with SANGER sequencing2019-04-01