This page is part of the Genetic Reporting Implementation Guide (v3.0.0: STU3) based on FHIR (HL7® FHIR® Standard) 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
Generated Narrative: Observation NOTCH1-significance
status: Final
category: Laboratory, Genetics
code: Diagnostic Implication
effective: 2023-02-01
performer: Practitioner Test Dolin
derivedFrom: Observation Genetic variant assessment
Code | Value[x] |
Genetic variation clinical significance [Imp] | Uncertain Significance |