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.

Livelast probed 2026-04-30 23:07Z· 105msCortexa

Status

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

Last probed: 1d ago
Last success: 1d ago
Last latency: 105ms

Schema

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

{
  "properties": {
    "variant": {
      "description": "Genomic variant in chr:pos:ref:alt format (GRCh38). Examples: '19:44908684:T:C' (APOE rs429358), '10:112998590:C:T' (TCF7L2 rs7903146). Also accepts chr-pos-ref-alt format.",
      "type": "string"
    }
  },
  "required": [
    "variant"
  ],
  "type": "object"
}

Examples (1)

Default FinnGen Get Variant Finemapping call

public-safeinput

{
  "variant": ""
}

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

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