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gnomAD

A specialized MCP server that interfaces with the Genome Aggregation Database (gnomAD) GraphQL API to provide genomic variant data, population frequencies, and gene constraint metrics. It enables AI assistants to perform clinical genetics research and population genomics analysis across multiple reference genomes.

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Forks
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Tools
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Updated
Aug 13, 2025
Validated
Jan 24, 2026

gnomAD MCP Server

A Model Context Protocol (MCP) server that provides access to the gnomAD (Genome Aggregation Database) GraphQL API. This server enables AI assistants to query genetic variant data, gene constraints, and population genetics information from gnomAD.

Features

  • 🧬 Gene Information: Search and retrieve detailed gene data including constraint scores
  • 🔬 Variant Analysis: Query specific variants and their population frequencies
  • 📊 Population Genetics: Access allele frequencies across different populations
  • 🧮 Constraint Scores: Get pLI, LOEUF, and other constraint metrics
  • 🔍 Region Queries: Find variants within specific genomic regions
  • 🧪 Transcript Data: Access transcript-specific information and constraints
  • 📈 Coverage Data: Retrieve sequencing coverage statistics
  • 🔄 Structural Variants: Query structural variant data
  • 🧲 Mitochondrial Variants: Access mitochondrial genome variants

Installation

Prerequisites

  • Node.js 18 or higher
  • npm or yarn

Install from source

git clone https://github.com/yourusername/gnomad-mcp-server.git
cd gnomad-mcp-server
npm install
npm run build

Configuration

Claude Desktop

Add to your Claude Desktop configuration file:

macOS: ~/Library/Application Support/Claude/claude_desktop_config.json Windows: %APPDATA%\Claude\claude_desktop_config.json

{
  "mcpServers": {
    "gnomad": {
      "command": "node",
      "args": ["/path/to/gnomad-mcp-server/dist/index.js"]
    }
  }
}

With MCP CLI

npx @modelcontextprotocol/cli gnomad-mcp-server

Available Tools

1. search

Search for genes, variants, or regions in gnomAD.

Parameters:

  • query (required): Search query (gene symbol, gene ID, variant ID, rsID)
  • reference_genome: Reference genome (GRCh37 or GRCh38, default: GRCh38)
  • dataset: Dataset ID (gnomad_r4, gnomad_r3, gnomad_r2_1, etc., default: gnomad_r4)

Example:

{
  "query": "TP53",
  "reference_genome": "GRCh38"
}

2. get_gene

Get detailed information about a gene including constraint scores.

Parameters:

  • gene_id: Ensembl gene ID (e.g., ENSG00000141510)
  • gene_symbol: Gene symbol (e.g., TP53)
  • reference_genome: Reference genome (default: GRCh38)

Example:

{
  "gene_symbol": "BRCA1",
  "reference_genome": "GRCh38"
}

3. get_variant

Get detailed information about a specific variant.

Parameters:

  • variant_id (required): Variant ID in format: chr-pos-ref-alt (e

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