{
  "record": {
    "id": "275978829b0b",
    "label": "IndiPGx-Pop p101",
    "cohort": "india-sim",
    "source": "report",
    "createdAt": "2026-10-30T13:56:21.696Z"
  },
  "calls": [
    {
      "gene": "CYP2C19",
      "diplotype": "*1/*2",
      "phenotype": "Intermediate Metabolizer",
      "source": "OUTSIDE"
    }
  ],
  "extract": {
    "genes": [
      {
        "activityScore": "",
        "diplotype": "*1/*2",
        "gene": "CYP2C19",
        "phenotype": "",
        "verbatim": "CYP2C19 rs4244285 G/A Heterozygous; CYP2C19 rs4986893 G/G Wild type; CYP2C19 rs12248560 C/C Wild type. Genotypes are reported per rsID on the forward strand. Star-allele assignment is left to the treating clinician."
      }
    ],
    "labName": "Sample Molecular Diagnostics, Bengaluru - NOT A REAL LAB",
    "methodNotes": "Genotypes are reported per rsID on the forward strand. Star-allele assignment is left to the treating clinician. Method: targeted genotyping by real-time PCR. Only the listed variants are assayed; variants outside this panel cannot be excluded.",
    "patientRef": "",
    "reportDate": "13 Oct 2026",
    "testedVariants": [
      {
        "gene": "CYP2C19",
        "variant": "rs4244285"
      },
      {
        "gene": "CYP2C19",
        "variant": "rs4986893"
      },
      {
        "gene": "CYP2C19",
        "variant": "rs12248560"
      }
    ],
    "warnings": [
      "Only the listed variants are assayed; variants outside this panel cannot be excluded.",
      "Star-allele assignment was left to the treating clinician; *1/*2 inferred from rsID mapping: rs4244285 het -> *2, rs4986893 wild type, rs12248560 wild type.",
      "Synthetic document generated for software benchmarking. Not a real patient or laboratory."
    ]
  },
  "quality": {
    "identifierRemoved": true,
    "unread": [],
    "coverage": [
      {
        "gene": "CYP2C19",
        "variant": "*2",
        "stated": true,
        "why": "Common no-function allele in South Asians"
      },
      {
        "gene": "CYP2C19",
        "variant": "*17",
        "stated": true,
        "why": "Increased-function allele"
      }
    ],
    "warnings": [
      "Only the listed variants are assayed; variants outside this panel cannot be excluded.",
      "Star-allele assignment was left to the treating clinician; *1/*2 inferred from rsID mapping: rs4244285 het -> *2, rs4986893 wild type, rs12248560 wild type.",
      "Synthetic document generated for software benchmarking. Not a real patient or laboratory."
    ]
  },
  "review": null,
  "pharmcat": {
    "version": "3.4.0",
    "data": "2026-07-13-11-40"
  },
  "note": "Research record. Not medical advice."
}