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MCP servers tagged variant-interpretation
7 live MCP servers tagged "variant-interpretation", ranked by trust score. Tags come from package metadata and repository topics, so this list covers servers across every category that work with variant-interpretation.
Autopvs1 Link
MCP server for AutoPVS1: automated ACMG PVS1 loss-of-function evidence for sequence variants and copy-number variants — variant interpretation as typed tools for LLM agents.
Litvar Link
MCP server for NCBI LitVar2: search the biomedical literature by genetic variant — the index linking variants to the publications that mention them, as typed tools for LLM agents.
Gnomad Link
MCP server for gnomAD (Genome Aggregation Database): variant allele frequencies, gene constraint, coverage, structural and mitochondrial variants, and liftover — as typed tools fo…
Mavedb Link
MCP server for MaveDB: quantitative variant-effect scores from Multiplexed Assays of Variant Effect (MAVE) and deep mutational scanning — functional evidence as typed tools for LL…
Spliceailookup Link
MCP server for SpliceAI Lookup (Broad Institute): SpliceAI, Pangolin and SpliceAI-10k splice-impact predictions for variants, plus an Ensembl VEP-backed variant resolver.
Clingen Link
MCP server for ClinGen (Clinical Genome Resource): gene–disease validity, dosage sensitivity, clinical actionability, and expert-panel variant pathogenicity (ERepo) — as typed too…
Metadome Link
MCP server for MetaDome: per-position missense tolerance (dN/dS) landscapes for human transcripts, Pfam domains, meta-domain homolog aggregation, and gnomAD/ClinVar per-position c…