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      "type": "VariantPathogenicityInterpretationGuideline",
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      "label": "pulmonary arterial hypertension",
      "type": "GeneticCondition"
    },
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              },
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              "type": "Criterion"
            },
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        ],
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                "type": "Contribution"
              }
            ],
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              },
              "id": "0080",
              "label": "BP4",
              "type": "Criterion"
            },
            "evidenceLine": [
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                    ],
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        ],
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              },
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              "label": "BA1",
              "type": "Criterion"
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              }
            ],
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              },
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            },
            "evidenceLine": [
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                    ],
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            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA2061382/MONDO:0015924/125/0/1804",
        "type": "EvidenceLine"
      },
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        "evidenceItem": [
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              {
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                },
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                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0079",
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000327",
                "id": "SEPIO:0000327",
                "label": "Benign Supporting"
              },
              "id": "0079",
              "label": "BP7",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
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                        },
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                          "description": "Date on which this evidence was provided"
                        },
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                        },
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                      }
                    ],
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                ],
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            ],
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            },
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          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA2061382/MONDO:0015924/125/0/1654",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA2061382/MONDO:0015924/125",
    "metadata": {
      "created": "2024-09-28T04:34:35.750Z",
      "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 04:34:35 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.0.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA26334-5",
      "id": "LN:LA26334-5",
      "label": "Likely Benign"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "31b37b7a-c652-4665-b6e0-a563c20d152d",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA2061382",
      "id": "CAR:CA2061382",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_001204.7:c.1512T>G"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_001204.7(BMPR2):c.1512T>G (p.Leu504=)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-10-14T16:58:13.373Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}