A sequence variant (rsID)

Extraits de code

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

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

$ch = curl_init("https://api.oanor.com/ensembl-api/v1/variant");
curl_setopt($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/ensembl-api/v1/variant",
    headers={"x-oanor-key": "oanor_test_..."}
)

Exemple de réponse

Une réponse réelle de ce endpoint, capturée lors du dernier contrôle de santé.

{
    "data": {
        "variant": {
            "name": "rs699",
            "source": "Variants (including SNPs and indels) imported from dbSNP",
            "evidence": [
                "Frequency",
                "1000Genomes",
                "Cited",
                "ESP",
                "Phenotype_or_Disease",
                "ExAC",
                "TOPMed",
                "gnomAD"
            ],
            "mappings": [
                {
                    "end": 230710048,
                    "start": 230710048,
                    "strand": 1,
                    "assembly": "GRCh38",
                    "location": "1:230710048-230710048",
                    "allele_string": "A/G",
                    "seq_region_name": "1"
                }
            ],
            "synonyms": [
                "106150.0001",
                "RCV000405686",
                "RCV000019691",
                "RCV000019693",
                "RCV000242838",
                "VCV000018068",
                "RCV000835695",
                "RCV002259306",
                "RCV000019692",
                "rs3182295",
                "rs17856353",
                "rs386606420",
                "rs4714",
                "rs61617185",
                "NM_001384479.1:c.776T>C",
                "NM_001382817.2:c.776T>C",
                "NM_001382817.1:c.803T>C",
                "NM_000029.3:c.803T>C",
                "NP_001371408.1:p.Met259Thr",
                "NM_000029.4:c.803T>C"
            ],
            "ambiguity": "R",
            "var_class": "SNP",
            "minor_allele": null,
            "minor_allele_freq": null,
            "clinical_significance": [
                "benign"
            ],
            "most_severe_consequence": "missense_variant"
        }
    },
    "meta": {
        "timestamp": "2026-06-01T08:14:18.547Z",
        "request_id": "256592f1-f1c4-40c4-8573-359d3e2b14ab"
    },
    "status": "ok",
    "message": "Variant retrieved",
    "success": true
}