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      "type": "VariantPathogenicityInterpretationGuideline",
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      "id": "MONDO:0015630",
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      "type": "GeneticCondition"
    },
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              "id": "0040",
              "label": "PP1",
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        "id": "CG-PCER-VARINT:CA383503778/MONDO:0015630/081/0/1630",
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                "id": "SEPIO:0000216",
                "label": "Pathogenic Moderate"
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              "id": "0018",
              "label": "PP4",
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        "id": "CG-PCER-VARINT:CA383503778/MONDO:0015630/081/0/1831",
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                "type": "Contribution"
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            ],
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              "@id": "https://obofoundry.org/sepio/clingen/0062",
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000329",
                "id": "SEPIO:0000329",
                "label": "Pathogenic Supporting"
              },
              "id": "0062",
              "label": "PP3",
              "type": "Criterion"
            },
            "evidenceLine": [
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                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA383503778/MONDO:0015630/081/el/0/1747/1749",
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              "label": "Met"
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                  "label": "curator role",
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                "type": "Contribution"
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            ],
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                "id": "SEPIO:0000329",
                "label": "Pathogenic Supporting"
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              "id": "0030",
              "label": "PM2",
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                    ],
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                ],
                "id": "CG-PCER-VARINT:CA383503778/MONDO:0015630/081/0/1636/1638",
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            ],
            "id": "CG-PCER-VARINT:CA383503778/MONDO:0015630/081/1/1637",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
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          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA383503778/MONDO:0015630/081/0/1636",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA383503778/MONDO:0015630/081",
    "metadata": {
      "created": "2024-09-28T05:28:43.066Z",
      "note": "DISCLAIMER: While the data/content in this document is approved by ClinGen expert panel(s), the SEPIO schema presented here is an initial prototype and has not been reviewed nor finalized by the ClinGen Data Exchange Modeling Team. We expect it to differ significantly from the final schema.",
      "producedAtUTC": "Sat, 28 Sep 2024 05:28:42 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.0.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA26332-9",
      "id": "LN:LA26332-9",
      "label": "Likely Pathogenic"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "2af4a425-9cc1-4fdf-b9c8-e03d528eaedf",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA383503778",
      "id": "CAR:CA383503778",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000552.5:c.4225G>T"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000552.5:c.4225G>T"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-10-27T00:13:29.904Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}