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 Observation: Pgx-var-1020

Generated Narrative

Resource "Pgx-var-1020"

Profile: Variant

status: final

category: Laboratory (Observation Category Codes#laboratory)

code: Genetic variant assessment (LOINC#69548-6)

subject: Patient/CGPatientExample01 " EVERYMAN"

effective: 2020-01-01

value: Present (LOINC#LA9633-4)

note: This variant was confirmed with SANGER sequencing

method: Sequencing (LOINC#LA26398-0)

component

code: Genomic reference sequence [ID] (LOINC#48013-7)

value: b37 Chr10 (nuccore#NC_000010.10)

component

code: Genomic coordinate system [Type] (LOINC#92822-6)

value: 1-based character counting (LOINC#LA30102-0)

component

code: Genomic allele start-end (LOINC#81254-5)

value: 96702047-96702047

component

code: Genomic ref allele [ID] (LOINC#69547-8)

value: C

component

code: Genomic alt allele [ID] (LOINC#69551-0)

value: C

component

code: Genomic source class [Type] (LOINC#48002-0)

value: Germline (LOINC#LA6683-2)

component

code: Allelic state (LOINC#53034-5)

value: homozygous (LOINC#LA6705-3)

component

code: Gene studied [ID] (LOINC#48018-6)

value: CYP2C9 (geneId#HGNC:2623)

component

code: DNA Change Type (LOINC#48019-4)

value: wild type (sequenceontology.org#SO:1000002)

component

code: Allelic read depth (LOINC#82121-5)

value: >20

component

code: Variant Confidence Status (To Be Determined Codes#variant-confidence-status)

value: High (Variant Confidence Status Codes#high)