A
licenseNot graded
qualityC
maintenanceEnables querying the gnomAD genome aggregation database for variant, gene, and region information.
4 npm
MIT
gnomAD MCP Server
by koido
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TDQS
B3.4/5.0
Scored across 12 tools
Disambiguation5/5
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.
Naming Consistency4/5
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.
Tool Count5/5
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.
Completeness4/5
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.
Maintenance
ActivityInactive
ResponsivenessNo issues