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Cortexa research tool·genomics·finngen
FinnGen Get Variant Finemapping
Get fine-mapping regions associated with a genomic variant in FinnGen. Returns phenotypes where this variant appears in a credible set from statistical fine-mapping. Input variant in chr:pos:ref:alt format (GRCh38). Useful for understanding which disease associations a variant contributes to in the Finnish population.
AvailableCortexa
Schema
JSON Schema the agent (or your API call) must match.
JSON · 12 lines · 323 chars
Examples (1)
Default FinnGen Get Variant Finemapping call
public-safeinput
JSON · 3 lines · 19 chars
Expected response keys: success
Anonymous-safe example. Rate-limited; no sign-in required.
Identifiers
- Catalog ID
- tu_FinnGen_get_variant_finemapping
- Tool name
- FinnGen_get_variant_finemapping
- Added
- 2026-04-30 22:47Z
- Tags
- tooluniverse