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Cortexa research tool·clinical·finngen
FinnGen Get Phenotype
Get detailed information about a specific FinnGen disease endpoint (phenotype). Returns case/control counts, genomic control lambda values, and genome-wide significant loci count for a given phenocode. Use phenocodes from FinnGen_list_phenotypes (e.g., 'T2D' for type 2 diabetes, 'I9_CHD' for coronary heart disease, 'C3_BREAST' for breast cancer).
AvailableCortexa
Schema
JSON Schema the agent (or your API call) must match.
JSON · 12 lines · 275 chars
Examples (1)
Default FinnGen Get Phenotype call
public-safeinput
JSON · 3 lines · 21 chars
Expected response keys: success
Anonymous-safe example. Rate-limited; no sign-in required.
Identifiers
- Catalog ID
- tu_FinnGen_get_phenotype
- Tool name
- FinnGen_get_phenotype
- Added
- 2026-05-01 00:58Z
- Tags
- tooluniverse