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      "type": "VariantPathogenicityInterpretationGuideline",
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      "id": "MONDO:0700270",
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      "type": "GeneticCondition"
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                ],
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            "statementOutcome": {
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              "label": "Not Met"
            },
            "type": "CriterionAssessment"
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        ],
        "evidenceStrength": {
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        },
        "id": "CG-PCER-VARINT:CA10579189/MONDO:0700270/020/0/1798",
        "type": "EvidenceLine"
      },
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        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA10579189/MONDO:0700270/020/el/0/1594",
        "evidenceItem": [
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                },
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                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
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            "evidenceLine": [
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                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA10579189/MONDO:0700270/020/el/0/1594/1596",
                "evidenceItem": [
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        },
        "id": "CG-PCER-VARINT:CA10579189/MONDO:0700270/020/0/1594",
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                    ],
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                "type": "EvidenceLine"
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            ],
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            "statementOutcome": {
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              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
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          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA10579189/MONDO:0700270/020/0/1774",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA10579189/MONDO:0700270/020",
    "metadata": {
      "created": "2026-04-10T19:18:54.945Z",
      "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": "Fri, 10 Apr 2026 17:40:54 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.0.0"
    },
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      "@id": "https://loinc.org/LA6668-3",
      "id": "LN:LA6668-3",
      "label": "Pathogenic"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "fd6e3003-802d-4057-8802-07351d5c8659",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA10579189",
      "id": "CAR:CA10579189",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000051.4:c.5631_5635delinsA"
            }
          ],
          "preferred": true
        },
        {
          "alleleName": [
            {
              "name": "NM_000051.4:c.5631_5635delCTCGCinsA"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000051.4(ATM):c.5631_5635delinsA (p.Phe1877fs)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-07-30T15:31:09.055Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}