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Source1

{
  "resourceType": "Observation",
  "id": "mii-exa-molgen-variante-2",
  "meta": {
    "profile": [
      "https://www.medizininformatik-initiative.de/fhir/ext/modul-molgen/StructureDefinition/variante|2026.0.4",
      "http://hl7.org/fhir/uv/genomics-reporting/StructureDefinition/variant|3.0.0"
    ]
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        "system": "http://loinc.org",
        "code": "69548-6",
        "display": "Genetic variant assessment"
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  },
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    "reference": "Patient/mii-exa-molgen-patient-2"
  },
  "effectiveDateTime": "2022-03-16",
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        "code": "LA26398-0",
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        "code": "86206-0",
        "display": "Whole genome sequence analysis in Blood or Tissue by Molecular genetics method"
      }
    ]
  },
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    "reference": "Specimen/mii-exa-molgen-specimen-2"
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  "device": {
    "reference": "Device/mii-exa-molgen-device-sequencer-2"
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            "code": "48005-3",
            "display": "Amino acid change (pHGVS)"
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            "code": "p.(Pro736Glnfs*58)"
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}