
Connects Claude to MyVariant.info, a genomics database aggregating variant annotations from dozens of sources. Right now it exposes one tool for fetching dataset metadata like build versions, source lists, and total variant counts. Part of the Pipeworx gateway ecosystem, so you can either hit this specific endpoint or connect to the full gateway for 784+ data sources. Includes an ask_pipeworx wrapper that lets you query in plain English instead of calling tools directly. Useful if you're building genetics research workflows and need programmatic access to variant database stats without hitting the MyVariant API yourself.
Sponsors
MyVariant.info MCP. Aggregated human genetic-variant annotation: dbSNP, ClinVar clinical significance, CADD/dbNSFP deleteriousness scores, gnomAD allele frequencies. Keyless BioThings API (sibling of MyGene.info). Docs: https://docs.myvariant.info/en/latest/
Part of Pipeworx — an MCP gateway connecting AI agents to 1865+ live data sources. This is an independent, unofficial integration — not affiliated with, endorsed by, or published by the upstream provider.
| Tool | Description |
|---|---|
query | Search aggregated human genetic-variant annotations on MyVariant.info. Accepts an rsID ("rs58991260") or a fielded query ("dbnsfp.genename:CDK2", "clinvar.rcv.clinical_significance:pathogenic"). A bare HGVS id does NOT match here — look one up with the variant tool instead. Each hit merges dbSNP, ClinVar clinical significance, CADD/dbNSFP deleteriousness scores, and gnomAD population allele frequencies. Returns { total, hits, assembly }; hit._id is the HGVS id you can pass to the variant tool, and its coordinates are in the assembly you asked for — hg19 unless you say otherwise. |
variant | Get the full merged annotation for a single human genetic variant by its HGVS id (e.g. "chr7:g.140453136A>T"). COORDINATES ARE hg19/GRCh37 BY DEFAULT — pass assembly "hg38" for GRCh38 positions, which is what gnomAD and Ensembl hand you. Returns annotations aggregated from dbSNP, ClinVar (pathogenicity / clinical significance), CADD and dbNSFP (deleteriousness/conservation scores), and gnomAD (population allele frequencies). Use to look up a known variant and read its pathogenicity and population frequency. |
metadata | Returns MyVariant.info build metadata: total indexed variant count, available annotation sources (dbSNP, ClinVar, CADD, dbNSFP, gnomAD), and their current release/build versions. |
Add to your MCP client (Claude Desktop, Cursor, Windsurf, etc.):
{
"mcpServers": {
"myvariant": {
"url": "https://gateway.pipeworx.io/myvariant/mcp"
}
}
}
tools/list at https://gateway.pipeworx.io/myvariant/mcp returns the tools in the table
above plus the shared Pipeworx meta-tools — ask_pipeworx,
discover_tools, search_within, remember/recall and the rest of the
gateway-wide set. So the tool count you see is larger than this table: a
single-pack endpoint currently lists roughly 30 shared tools alongside the
pack's own. The connection's initialize response states its exact scope, and
is the authoritative answer for a given day.
This is deliberate, not multiplexing by accident. The meta-tools are what let a
scoped connection answer a question this pack does not cover — via
ask_pipeworx, which routes across the whole catalog — without you adding a
second MCP server. There is currently no way to mount a pack endpoint without
them; if the extra schemas cost you more context than the routing is worth,
connect to the full gateway once rather than to several pack endpoints.
Or connect to the full Pipeworx gateway to get every pack's tools listed directly, instead of just this one's:
{
"mcpServers": {
"pipeworx": {
"url": "https://gateway.pipeworx.io/mcp"
}
}
}
Both URLs reach the same gateway and the same 1865+ data sources. The
only difference is which pack's tools are listed directly; ask_pipeworx
reaches all of them from either one.
curl -X POST https://gateway.pipeworx.io/v1/tools/myvariant_query \
-H 'Content-Type: application/json' \
-d '{"query":"rs58991260"}'
No account needed for the first calls. Inspect any tool: GET https://gateway.pipeworx.io/v1/tools/myvariant_query. Find one: POST https://gateway.pipeworx.io/v1/tools/search_packs with {"query":"..."}.
@pipeworx/mcp-myvariant is a local stdio bridge to the Pipeworx gateway: your MCP client
starts it with npx, and it forwards every call to the same
https://gateway.pipeworx.io/myvariant/mcp endpoint shown above. It needs network access;
there is no offline mode.
{
"mcpServers": {
"myvariant": {
"command": "npx",
"args": ["-y", "@pipeworx/mcp-myvariant"]
}
}
}
Without a key it calls anonymously, capped at 50 calls a day. A free account
raises that to 200 a day: get a key at https://pipeworx.io/signup and add
"env": { "PIPEWORX_API_KEY": "<your key>" } to the server entry.
The key is sent as a Bearer token, the same way a hosted connection sends it,
so calls are metered and billed exactly as they are there.
It lists only this pack's tools by default. Set PIPEWORX_META_TOOLS=1 to
also list ask_pipeworx and the other gateway-wide tools.
Behind an HTTPS proxy: Node's built-in fetch does not read HTTPS_PROXY by
default. Newer Node releases honour it when NODE_USE_ENV_PROXY=1 is set; check
your Node version's documentation.
Instead of calling tools directly, you can ask questions in plain English — this works on the pack endpoint above as well as on the full gateway:
ask_pipeworx({ question: "your question about Myvariant data" })
The gateway picks the right tool and fills the arguments automatically.
MIT