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      "label": "ClinGen PAH Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 1",
      "type": "VariantPathogenicityInterpretationGuideline",
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      "type": "GeneticCondition"
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              "id": "0011",
              "label": "PM2",
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                "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006/0/1798/1800",
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            ],
            "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006/1/1799",
            "statementOutcome": {
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        "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006/0/1798",
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            ],
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000220",
                "id": "SEPIO:0000220",
                "label": "Pathogenic Very Strong"
              },
              "id": "0017",
              "label": "PVS1",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA891843538/MONDO:0009861/006/el/0/1594/1596",
                "evidenceItem": [
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                          "description": "Date on which this evidence was provided"
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                    ],
                    "id": "CA891843538/MONDO:0009861/006/ci/CA891843538/MONDO:0009861/006.002",
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                ],
                "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006/0/1594/1596",
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            ],
            "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006/1/1595",
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              "@id": "SEPIO:0000224",
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            },
            "type": "CriterionAssessment"
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        },
        "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006/0/1594",
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            "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA891843538/MONDO:0009861/006/ei/1/1634",
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                },
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                },
                "type": "Contribution"
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            ],
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              "@id": "https://obofoundry.org/sepio/clingen/0063",
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000329",
                "id": "SEPIO:0000329",
                "label": "Pathogenic Supporting"
              },
              "id": "0063",
              "label": "PP4",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA891843538/MONDO:0009861/006/el/0/1633/1635",
                "evidenceItem": [
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            ],
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000216",
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              },
              "id": "007",
              "label": "PM3",
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                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA891843538/MONDO:0009861/006/el/0/1717/1719",
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                        },
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                          "description": "Date on which this evidence was provided"
                        },
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                          "id": "SEPIO:0000516",
                          "label": "curator role",
                          "type": "ContributoryRole"
                        },
                        "type": "Contribution"
                      }
                    ],
                    "id": "CA891843538/MONDO:0009861/006/ci/CA891843538/MONDO:0009861/006.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006/0/1717/1719",
                "type": "EvidenceLine"
              }
            ],
            "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006/1/1718",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Not Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006/0/1717",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA891843538/MONDO:0009861/006",
    "metadata": {
      "created": "2024-09-28T01:28:44.762Z",
      "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 01:28:44 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.0.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA6668-3",
      "id": "LN:LA6668-3",
      "label": "Pathogenic"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "80f0708e-fa2a-4625-be82-9937dbc9ae51",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA891843538",
      "id": "CAR:CA891843538",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000277.3:c.686dup"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000277.3(PAH):c.686dup (p.Asp229fs)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-11-04T19:40:23.834Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}