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 RiskAssessment: GenRiskDiabetesT2

Generated Narrative

Resource "GenRiskDiabetesT2"

parent: Observation/PolyGenicDiagnosticImpExample

status: final

subject: Patient/CGPatientExample01 " EVERYMAN"

basis:

  • : Variant 1
  • : Variant 2
  • : Variant 3
  • : Variant 4
  • : Variant 5
  • : Variant 6
  • : Variant 7

prediction

outcome: Diabetes mellitus type 2 (disorder) (SNOMED CT#44054006)

probability: 0.26

qualitativeRisk: Low likelihood (Risk Probability#low)

relativeRisk: 1.05

when: ?-53

prediction

outcome: Diabetes mellitus type 2 (disorder) (SNOMED CT#44054006)

probability: 0.7

qualitativeRisk: High likelihood (Risk Probability#high)

relativeRisk: 2.69

when: ?-65