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Cortexa connector·genomics
ClinVar
Search ClinVar for clinical significance of genetic variants. Use for variant pathogenicity, allele frequency, and condition associations.
AvailableClinVar
Schema
JSON Schema the agent (or your API call) must match.
JSON · 22 lines · 498 chars
Examples (1)
Search ClinVar
public-safeinput
JSON · 4 lines · 36 chars
Expected response keys: count, results, source
Anonymous-safe example. Rate-limited; no sign-in required.
Identifiers
- Catalog ID
- search_clinvar
- Source ID
- clinvar
- Vertical
- genomics
- Added
- 2026-04-30 22:47Z
- Tags
- direct