Pharmacogenomics Guidelines MCP Server
Find pharmacogenomics guidelines, translate diplotypes, and retrieve prescribing recommendations.
Connector by cyanheads · GitHub account verified by the MCP Registry
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Install
Works with Claude Code, Codex, VS Code, Cursor, Windsurf, Claude Desktop. Read the repository before you give any tool access to your data.
npx agentmarket install connector/cyanheads-pharmacogenomics-guidelines-mcp-server
Asks which of your tools to add it to (Claude Code, Codex, Cursor, VS Code, Windsurf, Gemini CLI, Claude Desktop) and shows the change first. See https://agentmart.dev/cli.
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About
Reviews
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Permissions
What this server can do and what it asks for, from its tool list and install config. Checked Oct 25, 2026.
- Tools
- 6 read · 0 write · 0 deleteRead-only
- Secrets
- None asked for
- Install scripts
- Not scanned yet
- Runs as
- Node.js package
Tools by what they do 6
Read from the source code; the running server may list different tools.
Read 6 · Look things up without changing anything.
pgx_get_guidelinepgx_get_recommendationspgx_list_referencepgx_lookup_diplotypepgx_search_allelespgx_search_pairs
Secrets and settings it asks for
Other settings (environment variables or headers).
MCP_LOG_LEVEL
Tools (6)
Read from the source code; the running server may differ. Descriptions are the server’s own words; hidden characters are shown as [U+…].
pgx_get_guidelineGet guideline coverageread-onlyRetrieve guideline coverage by source ID, exact gene symbol or exact drug name/ID. Default summary pages complete guideline records with exact drugCount/pairCount. view=drugs or pairs requires by=id and pages only that related collection, retaining its guideline descriptor. Ambiguous drug names page candidates for retry with drugId. Follow page.nextOffset; the 24,000-byte soft budget cuts only between complete rows, with oversizedRow for an indivisible exception. Missing coverage is found=false. Consult linked guidelines before clinical use.
pgx_get_recommendationsGet recommendationsread-onlyBrowse CPIC recommendations in drug mode with one exact drugName or drugId. Match across drugs in results mode with geneResults or geneSymbol plus phenotype/activityScore, or genotype mode with 1–10 uniquely resolved gene/diplotype entries. Both matching modes accept an optional drug. Use pgx_list_reference topic phenotypes for source values. Every matched prerequisite must be explicit; omitted genes are never normal or negative. Preserve populations, scores, classifications and source text. Follow page.nextOffset and incompletePage.nextOffset independently; consult linked guidelines before cl…
pgx_list_referenceList pharmacogenomics reference valuesread-onlyInspect gene symbols, gene-specific source results, CPIC levels, ClinPGx testing labels, recommendation classifications and input formats. phenotypes requires geneSymbol and preserves distinct activity-score rows, frequencies and consultation text. Live genes/phenotypes support paging; static topics return their complete vocabulary without upstream requests. Use returned values in subsequent discovery, diplotype and recommendation calls.
pgx_lookup_diplotypeLook up diplotyperead-onlyTranslate a CPIC-supported diplotype or allele-status result for one gene. Supply geneSymbol and exact diplotype notation, including star alleles, named HLA positive/negative statuses, or non-star sequences; use pgx_search_alleles and pgx_list_reference with topic phenotypes to inspect supported values. Exact lookup precedes bounded reverse-order or status aliases. Multiple source rows remain ambiguous; no activity score or missing gene result is inferred.
pgx_search_allelesSearch allelesread-onlyInspect CPIC allele function, evidence, definition metadata and complete population frequencies for geneSymbol. Name matches literally first, then a matching gene prefix before a star allele may be removed; clinicalFunctionalStatus matches literal text case-insensitively. Discover genes with pgx_list_reference. Definitions are metadata, not variant interpretation. Frequencies are source fractions; inferred frequencies are not observations and do not establish individual risk. Pages have a 24,000-byte complete-result soft budget; an indivisible exception sets oversizedRow. Continue with page.ne…
pgx_search_pairsSearch evaluated gene–drug pairsread-onlySearch evaluated gene–drug pairs by gene, literal drug-name substring, exact drug/RxNorm/ATC identifiers, evaluation level or testing label. Filters combine with AND; identifiers never fall back to name-only search. Results include source drug identifiers and guideline links for pgx_get_guideline. A pair evaluation is not a prescribing recommendation. Follow nextOffset to continue.
Signals
- Stars
- 1
- Forks
- 0
- Open issues
- 0
- Weekly downloads
- 18
- Last commit
- Oct 20, 2026 (10 days ago)
- Last release
- Oct 20, 2026 (10 days ago)
- Last package publish
- Oct 20, 2026 (10 days ago)
From GitHub (fetched Oct 24, 2026) and the package registry.
Details
- Registry name
io.github.cyanheads/pharmacogenomics-guidelines-mcp-server- Version
- 0.2.0
- Auth
- No auth
- Packages
- npm @cyanheads/pharmacogenomics-guidelines-mcp-servernpm @cyanheads/pharmacogenomics-guidelines-mcp-server
- License
- Apache-2.0
- First seen
- Oct 24, 2026
- Last checked
- Oct 24, 2026
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Pharmacogenomics Guidelines MCP Server. Agent Mart. https://agentmart.dev/connectors/cyanheads-pharmacogenomics-guidelines-mcp-server (last updated 2026-10-24)