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Cortexa research tool·structure·ncbi_variation
NCBIVariation Rsid Lookup
Look up a dbSNP rsID and retrieve variant details including GRCh38 genomic coordinates, associated genes, clinical significance (ClinVar), citations, and MANE Select transcript IDs. Accepts rsID with or without 'rs' prefix (e.g., 'rs429358' or '429358'). Returns structured summary of the variant.
AvailableCortexa
Schema
JSON Schema the agent (or your API call) must match.
JSON · 12 lines · 288 chars
Examples (1)
Default NCBIVariation Rsid Lookup call
public-safeinput
JSON · 3 lines · 23 chars
Expected response keys: success
Anonymous-safe example. Rate-limited; no sign-in required.
Identifiers
- Catalog ID
- tu_NCBIVariation_rsid_lookup
- Tool name
- NCBIVariation_rsid_lookup
- Added
- 2026-04-30 22:47Z
- Tags
- tooluniverse