@pipeworx/myvariant

Connect: https://gateway.pipeworx.io/myvariant/mcp · Install: one-click buttons

Tools: 3

Tools

  • query — Search aggregated human genetic-variant annotations on MyVariant.info. Accepts an rsID (“rs58991260”), an HGVS id (“chr1:g.218631822G>A”), or a fielded query (“dbnsfp.genename:CDK2”, “clinvar.rcv.clin
  • variant — Get the full merged annotation for a single human genetic variant by its HGVS id (e.g. “chr7:g.140453136A>T”). Returns annotations aggregated from dbSNP, ClinVar (pathogenicity / clinical significance
  • 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 ), an HGVS id ( chr1:g.218631822G>A ), or a fielded query ( dbnsfp.genename:CDK2 , clinvar.rcv.clini
  • variant — Get the full merged annotation for a single human genetic variant by its HGVS id (e.g. chr7:g.140453136A>T ). Returns annotations aggregated from dbSNP, ClinVar (pathogenicity / clinical significance)

Regenerated from source · build July 21, 2026