A variant clinical summary

Code-Snippets

curl "https://api.oanor.com/clinvar-api/v1/variant" \
  -H "x-oanor-key: oanor_test_..."

await fetch("https://api.oanor.com/clinvar-api/v1/variant", {
  headers: { "x-oanor-key": "oanor_test_..." }
});

$ch = curl_init("https://api.oanor.com/clinvar-api/v1/variant");
curl_setopt($ch, CURLOPT_HTTPHEADER, ["x-oanor-key: oanor_test_..."]);
curl_setopt($ch, CURLOPT_RETURNTRANSFER, true);
$out = curl_exec($ch);

import requests
requests.get(
    "https://api.oanor.com/clinvar-api/v1/variant",
    headers={"x-oanor-key": "oanor_test_..."}
)

Beispiel-Response

Echte Antwort dieses Endpoints, erfasst beim letzten Health-Check.

{
    "data": {
        "variant": {
            "id": "4852102",
            "url": "https://www.ncbi.nlm.nih.gov/clinvar/variation/4852102/",
            "type": "copy number loss",
            "genes": [
                "BRCC3",
                "CLIC2",
                "CMC4",
                "F8",
                "FUNDC2",
                "LOC106146143"
            ],
            "title": "GRCh38/hg38 Xq28(chrX:154890748-155334361)x1",
            "location": "00000000000154890748",
            "accession": "VCV004852102",
            "chromosome": "X",
            "conditions": [
                "See cases"
            ],
            "cdna_change": "GRCh38/hg38 Xq28(chrX:154890748-155334361)x1",
            "primary_gene": "BRCC3",
            "review_status": "criteria provided, single submitter",
            "classification": "Pathogenic",
            "protein_change": null,
            "variation_name": "GRCh38/hg38 Xq28(chrX:154890748-155334361)x1",
            "classification_type": "germline",
            "molecular_consequence": []
        }
    },
    "meta": {
        "timestamp": "2026-06-01T16:23:33.933Z",
        "request_id": "38969713-5e4d-4140-9b89-26ec701998f8"
    },
    "status": "ok",
    "message": "Variant retrieved",
    "success": true
}