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 in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions

Example Observation: VariantExample2

Generated Narrative

Resource "VariantExample2"

Profile: Variant

status: final

category: Laboratory (Observation Category Codes#laboratory)

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

subject: Patient/CGPatientExample01 " EVERYMAN"

effective: 2019-04-01

value: Present (LOINC#LA9633-4)

method: Sequencing (LOINC#LA26398-0)

component

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

value: NC_000010.10 (nuccore#NC_000010.10)

component

code: Allelic State (LOINC#53034-5)

value: heterozygous (LOINC#LA6706-1)

component

code: Ref nucleotide (LOINC#69547-8)

value: C

component

code: Alt allele (LOINC#69551-0)

value: A

component

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

value: 96527334-?