Back to catalog
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.
View JSON schemaExpandCollapse
JSON · 22 lines · 498 chars
Examples (1)
Search ClinVar
Public-safe example · rate-limited
JSON input · 4 lines · 36 chars
Expected response keys: count, results, source
Identifiers
- Catalog ID
- search_clinvar
- Source ID
- clinvar
- Vertical
- genomics
- Added
- 2026-04-30 22:47Z
- Tags
- direct