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Query gene variant annotations and related data for research and analysis.
Copy the install command and let the AI configure it · recommended for beginners
Please install the "Myvariant" MCP server from askskill: Run: claude mcp add --transport http 'io-github-pipeworx-io-myvariant' 'https://gateway.pipeworx.io/myvariant/mcp'
Use MyVariant.info to query variant chr7:g.140453136A>T and return its gene, protein impact, clinical significance, and major database annotations.
A structured annotation result with the mapped gene, functional impact, and a summary of clinical relevance.
Use MyVariant.info to batch query these variants: chr17:g.43045702A>G, chr13:g.32340328G>A, and chr7:g.140453136A>T, then format the results as a table with gene name, variant type, and pathogenicity information.
A comparison-ready summary table showing annotations and potential risk signals across multiple variants.
Use MyVariant.info to find variant annotation data related to BRCA1, and summarize common high-impact variants and their clinical database sources.
An overview of key variants linked to the target gene, including data sources and annotation highlights.
Annotate whole-genome VCFs and query pharmacogenomics and disease risk in natural language.
Retrieve disease-related information for fast medical lookup and research.
Query MGI mouse genetics data for markers, mutations, phenotypes, and disease models.
Annotate genetic variants and predict functional effects via the Ensembl VEP API.
Query genes, sequences, variant effects, orthologs, and annotations via Ensembl.
Access cBioPortal to explore cancer genomics alterations and cohort data.