@pipeworx/myvariant

Connect: https://pipeworx.io/mcp — every tool in the catalog, including @pipeworx/myvariant’s. Install: one-click buttons

Connect to just the @pipeworx/myvariant pack

https://gateway.pipeworx.io/myvariant/mcp — only @pipeworx/myvariant’s own tools, nothing else in the catalog.

No MCP client? Skip the connection: POST https://gateway.pipeworx.io/v1/tools/search_packs {"query":"..."} to find a tool below, GET /v1/tools/<name> for its schema, POST the same URL with arguments for the data — see For AI agents.

Tools: 3

Tools

  • 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 bar
  • 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
  • metadata — Returns MyVariant.info build metadata: total indexed variant count, available annotation sources (dbSNP, ClinVar, CADD, dbNSFP, gnomAD), and their current release/build versions.

Tools

  • metadata — Returns MyVariant.info build metadata: total indexed variant count, available annotation sources (dbSNP, ClinVar, CADD, dbNSFP, gnomAD), and their current release/build versions.
  • 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
  • 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

Regenerated from source · build October 22, 2026