gnomAD MCP Server
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Alternatives to gnomAD MCP Server
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Related Servers
- AlicenseNot gradedqualityBmaintenanceEnables querying the gnomAD genome aggregation database for variant, gene, and region information.363 npmMIT
- FlicenseBqualityDmaintenanceEnables AI assistants to query genetic variant data, gene constraints, and population genetics information from the gnomAD (Genome Aggregation Database) through its GraphQL API. Supports searching for genes and variants, retrieving constraint scores, analyzing population frequencies, and accessing genomic coverage data.910-
- AlicenseNot gradedqualityCmaintenanceEnables querying dbSNP refSNP records and converting between HGVS, SPDI, and rsID identifiers for human genetic variants, with assembly-aware genomic placement and population frequencies.63 npmMIT
- FlicenseAqualityFmaintenanceProvides interpretable variant effect predictions for 4.2 million ClinVar variants using the EVEE API. Enables searching, comparing, and analyzing genetic variants with AI-generated mechanistic interpretations and disruption profiles.618-
- AlicenseBqualityDmaintenanceProvides comprehensive access to the UCSC Genome Browser API, enabling queries of genomic data, DNA sequences, gene annotations, variants, and metadata across multiple species and assemblies.126MIT
- AlicenseNot gradedqualityCmaintenanceFederates 13 gene-related MCP backends (gnomAD, GTEx, etc.) behind a single Streamable HTTP endpoint with collision-free namespacing and search-based tool discovery.6MIT
TDQS
Scored across 12 tools
Each tool has a clearly distinct purpose targeting specific genomic data types (ClinVar variants, copy number variants, genes, metadata, mitochondrial variants, regions, STRs, structural variants, general variants, liftover, gene search, variant search). The descriptions clearly differentiate what each tool retrieves, with no apparent overlap in functionality.
Most tools follow a consistent 'get_*_info' or 'search_for_*' pattern, but there are minor deviations: 'get_copy_number_variant_info' uses 'variantId' while 'get_variant_info' uses 'variantId' (both camelCase), and 'get_structural_variant_info' uses 'variantId' while others use 'variant_id' (snake_case). The overall pattern is clear and readable despite these inconsistencies.
12 tools is well-scoped for a genomic database API server covering multiple data types (variants, genes, regions, etc.) across different gnomAD versions. Each tool serves a specific purpose in retrieving different genomic entities, with no obvious redundancy.
The toolset provides comprehensive retrieval capabilities for the gnomAD domain, covering all major genomic data types with both specific lookup and search functionality. The only minor gap is the version compatibility limitations noted in tool descriptions (some tools only work with specific gnomAD versions), but agents can work around this by checking metadata or using alternative tools.