variation

Active

declared in 0.1.0

"What is [rsID]" / "look up SNP [rs...]" / "variant info for [rsN]" — fetch a genetic variation record by ID (e.g. rs56116432). Returns alleles, genomic location, clinical significance, gene mappings. Use for SNP lookups, pharmacogenomics, GWAS follow-up.

Parameters schema

{
  "type": "object",
  "examples": [
    {
      "species": "human",
      "variant_id": "rs56116432"
    }
  ],
  "required": [
    "species",
    "variant_id"
  ],
  "properties": {
    "species": {
      "type": "string"
    },
    "variant_id": {
      "type": "string",
      "description": "e.g. \"rs56116432\""
    }
  }
}

What this tool wraps· 1 endpoint

min confidence0.70 0.50

Data resourceEnsembl Genome Browser
EMBL-EBI · scientific-data
name mention0.85

Parent server

Ensembl

https://github.com/pipeworx-io/mcp-ensembl

1/7 registries

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