Folklore Clinical Variant Interpretation MCP
Made in BulgariaBioinformatics MCP for genomic variant interpretation, gene-disease evidence and literature.
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What is Folklore Clinical Variant Interpretation MCP?
Folklore Clinical Variant Interpretation MCP is the free, public, read-only MCP interface from Helena Bioinformatics. It helps qualified genetics professionals and researchers interpret one supported GRCh38 germline SNV or simple indel, review ACMG/AMP evidence and source provenance, find ClinGen gene-disease associations, and retrieve scientific literature. Connect using Streamable HTTP at https://api.helena.bio/folklore/v1/mcp. No account or API key is required. The public adapter is available under Apache-2.0 at https://github.com/helena-bioinformatics/folklore-mcp. Results require qualified professional review. Do not submit patient records, family information or private case data. The MCP does not process VCF uploads, FASTQ or BAM files and does not provide patient diagnosis or treatment recommendations. The public MCP adapter launched in 2026.
Key features
Pros & cons
- No account or API key required
- Read-only public evidence with source provenance
- Official public adapter and client setup documentation
- Qualified genetics professional review required
- Variant interpretation limited to supported GRCh38 germline SNVs and simple indels smaller than 50 base pairs
- No patient records, VCF uploads or batch analysis
Who it's for
Frequently asked questions
Is Folklore Clinical Variant Interpretation MCP free?
Folklore Clinical Variant Interpretation MCP is free to use. Check the Folklore Clinical Variant Interpretation MCP website for current pricing.
What is Folklore Clinical Variant Interpretation MCP used for?
Bioinformatics MCP for genomic variant interpretation, gene-disease evidence and literature. Folklore Clinical Variant Interpretation MCP is the free, public, read-only MCP interface from Helena Bioinformatics. It helps qualified genetics professionals and researchers interpret one supported GRCh38 germline SNV or simple indel, review ACMG/AMP evidence and source provenance, find ClinGen gene-disease…
Who is Folklore Clinical Variant Interpretation MCP for?
Folklore Clinical Variant Interpretation MCP is built for Clinical geneticists, molecular geneticists, bioinformaticians, laboratory professionals and genomics researchers.
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