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).

Livelast probed 2026-05-01 01:00Z· 107msCortexa

Status

The most recent probe succeeded. Safe to call from the agent today.

Last probed: 1d ago
Last success: 1d ago
Last latency: 107ms

Schema

JSON Schema the agent (or your API call) must match.

{
  "properties": {
    "phenocode": {
      "description": "FinnGen phenotype code (e.g., 'T2D', 'I9_CHD', 'C3_BREAST', 'J10_ASTHMA'). Get valid codes from FinnGen_list_phenotypes.",
      "type": "string"
    }
  },
  "required": [
    "phenocode"
  ],
  "type": "object"
}

Examples (1)

Default FinnGen Get Phenotype call

public-safeinput

{
  "phenocode": ""
}

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

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