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Research tool·genomics·ncbi_variation
NCBIVariation Spdi To Rsids
Reverse lookup from a normalized SPDI variant to the co-located dbSNP rsID(s), using NCBI Variation Services /spdi/{spdi}/rsids. Complements the forward direction (rsid_lookup) and the SPDI conversion tools, letting you recover an rsID from a genomic SPDI/coordinate. SPDI format: 'SeqID:Position:DeletedSequence:InsertedSequence' (0-based interbase). Returns a list of integer rsIDs.
AvailableCortexa
Schema
JSON Schema the agent (or your API call) must match.
View JSON schemaExpandCollapse
JSON · 12 lines · 303 chars
Examples (1)
Default NCBIVariation Spdi To Rsids call
Public-safe example · rate-limited
JSON input · 3 lines · 41 chars
Expected response keys: success
Identifiers
- Catalog ID
- tu_NCBIVariation_spdi_to_rsids
- Tool name
- NCBIVariation_spdi_to_rsids
- Added
- 2026-07-29 18:13Z
- Tags
- tooluniverse