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    "@id": "https://cgerepoapi/evrepo/api/summary/classification/c8a91da2-ceea-4f18-96cd-b6e50647993d/doc/sepio/version/1.0.0",
    "assertionMethod": {
      "@id": "https://cspec.genome.network/cspec/SequenceVariantInterpretation/id/1807907463",
      "label": "ClinGen Limb Girdle Muscular Dystrophy Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for DYSF Version 1.0.0",
      "type": "VariantPathogenicityInterpretationGuideline",
      "version": "1.0.0"
    },
    "condition": {
      "@id": "https://api.monarchinitiative.org/api/bioentity/phenotype/MONDO:0015152",
      "id": "MONDO:0015152",
      "label": "autosomal recessive limb-girdle muscular dystrophy",
      "type": "GeneticCondition"
    },
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              "label": "Met"
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        "id": "CG-PCER-VARINT:CA1707668/MONDO:0015152/180/0/1636",
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              "label": "Met"
            },
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          }
        ],
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        "id": "CG-PCER-VARINT:CA1707668/MONDO:0015152/180/0/1669",
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        ],
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        "id": "CG-PCER-VARINT:CA1707668/MONDO:0015152/180/0/1738",
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            },
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        ],
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                    "id": "CA1707668/MONDO:0015152/180/ci/CA1707668/MONDO:0015152/180.002",
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                        "comments": "The computational predictor REVEL gives a score of 0.480 (PP3 and BP4 not met).\n\nSpliceAI 0",
                        "contributionDate": {
                          "date": "2025/10/9",
                          "description": "Date on which this evidence was provided"
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                "id": "CG-PCER-VARINT:CA1707668/MONDO:0015152/180/0/1747/1749",
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            ],
            "id": "CG-PCER-VARINT:CA1707668/MONDO:0015152/180/1/1748",
            "statementOutcome": {
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            },
            "type": "CriterionAssessment"
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        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA1707668/MONDO:0015152/180/0/1747",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA1707668/MONDO:0015152/180",
    "metadata": {
      "created": "2025-10-09T23:21:15.246Z",
      "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": "Thu, 09 Oct 2025 23:21:15 -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": "c8a91da2-ceea-4f18-96cd-b6e50647993d",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA1707668",
      "id": "CAR:CA1707668",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_001130987.2:c.6313G>A"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_001130987.2(DYSF):c.6313G>A (p.Ala2105Thr)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-10-28T20:28:47.620Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}