Broad Institute gnomAD genomic variant database (GraphQL)
Broad Institute gnomAD genomic variant database (GraphQL)
Gnomad · v0.1.0
by Pipeworx-io
48
mcp-gnomad
Broad Institute gnomAD genomic variant database (GraphQL)
Part of Pipeworx — an MCP gateway connecting AI agents to 250+ live data sources.
Tools
| Tool | Description |
|---|---|
variant |
Variant by chr-pos-ref-alt (e.g. "1-55051215-G-A") or rsid. |
gene |
Gene info + variants. Accepts gene symbol (e.g. "BRCA1") or Ensembl gene id. |
region |
Variants in a genomic region (≤25kb recommended). |
transcript |
Transcript + variants. |
search |
Gene / variant search (autocomplete). |
Quick Start
Add to your MCP client (Claude Desktop, Cursor, Windsurf, etc.):
{
"mcpServers": {
"gnomad": {
"url": "https://gateway.pipeworx.io/gnomad/mcp"
}
}
}
Or connect to the full Pipeworx gateway for access to all 250+ data sources:
{
"mcpServers": {
"pipeworx": {
"url": "https://gateway.pipeworx.io/mcp"
}
}
}
Using with ask_pipeworx
Instead of calling tools directly, you can ask questions in plain English:
ask_pipeworx({ question: "your question about Gnomad data" })
The gateway picks the right tool and fills the arguments automatically.
More
License
MIT