NestDaddy

GeneBe

net.genebe/genebe-mcp · v0.1.0

Annotate and classify human genetic variants with GeneBe (ACMG, gnomAD, ClinVar). Research use only.

Connect Remote server

Terminal
claude mcp add --transport http genebe-mcp https://mcp.genebe.net/v1/mcp
~/.cursor/mcp.json
{
  "mcpServers": {
    "genebe-mcp": {
      "url": "https://mcp.genebe.net/v1/mcp"
    }
  }
}
.vscode/mcp.json
{
  "servers": {
    "genebe-mcp": {
      "type": "http",
      "url": "https://mcp.genebe.net/v1/mcp"
    }
  }
}
Claude Desktop
Settings > Connectors > Add custom connector
URL: https://mcp.genebe.net/v1/mcp

Tools 6 found in our last check

  • annotate_variant

    Annotate and classify one human genetic variant using GeneBe. Start here for any question about a variant (what is it, is it pathogenic/benign, how common is it). Returns the ACMG verdict with points and criteria, population frequency (gnomAD), predictor scores (REVEL, AlphaMiss…

  • explain_acmg_decision_path

    Explain step by step why each classification criterion did or did not apply to a variant. Use after annotate_variant when the user asks "why was this classified that way?". Returns an ASCII rendering of the decision tree with the evaluated conditions. By default it explains the…

  • convert_variant

    Convert a variant written in any notation into normalized hg38 genomic coordinates. Use when you only need the chr/pos/ref/alt of a variant (for example to translate HGVS or an rsID), without annotation. Does not classify the variant; use annotate_variant for that.

  • get_variant_effects

    List a variant's predicted molecular consequences on every overlapping transcript. Returns per-transcript HGVS (c. and p.), consequence terms (e.g. missense_variant) and impact, most severe and MANE Select transcripts first. Lightweight: no frequencies or classification.

  • get_gene

    Look up a human gene: identifiers, location, MANE Select transcript, ClinGen gene-disease validity. Use for questions about a gene rather than a specific variant. Transcripts are listed with MANE Select first and capped; check total_transcripts.

  • liftover_coordinate

    Convert a genomic position, interval or variant between genome builds (hg19, hg38, t2t). Check `status`: RESOLVED means one result, AMBIGUOUS means several candidates, anything else means it could not be mapped (see errors). For variants, ref/alt are rebuilt against the target r…

Details

Endpointhttps://mcp.genebe.net/v1/mcp (Streamable HTTP)
First published22 Oct 2026
Last updated22 Oct 2026
Registry namenet.genebe/genebe-mcp

More other servers See all

Listing data from the official MCP registry. Status and tools from NestDaddy's daily check. Browse all MCP servers.