{"enrichment":{"faq":[{"a":"ClinPGx Database provides REST API access to pharmacogenomic annotations, CPIC and DPWG dosing guidelines, variant-drug associations, and drug label data. Search by gene symbol, drug name, or variant ID to retrieve clinical evidence levels, genotype-specific recommendations, and precision-medicine prescribing guidance for drug-gene interactions.","q":"What is the ClinPGx Database and what data does it provide?"},{"a":"ClinPGx Database offers two complementary endpoints to access clinical pharmacogenomics data. Query by gene symbol to find genetic variants affecting medication response and metabolism, search by drug name to retrieve associated PGx phenotypes and genotype-to-phenotype mappings, or use variant ID to access clinical evidence for precision medicine dosing recommendations.","q":"How do I look up pharmacogenomics clinical data in ClinPGx?"},{"a":"Yes. ClinPGx Database is designed to help you find genetic variants affecting medication response and metabolism. It provides access to clinical evidence for precision medicine dosing recommendations, PGx phenotypes, and genotype-to-phenotype mappings that support personalized medication selection and dosing based on individual genetic profiles.","q":"Can ClinPGx Database help find genetic drug response information?"},{"a":"ClinPGx Database integrates CPIC (Clinical Pharmacogenetics Implementation Consortium) and DPWG (Dutch Pharmacogenetics Working Group) dosing guidelines. These guidelines provide evidence-based recommendations for adjusting medication therapy based on pharmacogenomic test results and genetic biomarkers affecting drug response.","q":"What clinical guidelines does ClinPGx reference?"},{"a":"ClinPGx Database enables precision medicine by providing genotype-specific recommendations and clinical evidence levels for drug-gene interactions. Access pharmacogenomic annotations and drug label data to make informed dosing decisions tailored to patients' genetic profiles, improving medication efficacy and safety.","q":"How can ClinPGx Database support precision medicine prescribing?"}],"shadow_tags":["pharmacogenomics-reference","clinical-genetics","drug-metabolism","precision-medicine","pgx-variants","genetic-biomarkers","clinical-decision-support","medication-genomics"],"summary_rewrite":"ClinPGx Database provides REST API access to pharmacogenomic annotations, CPIC and DPWG dosing guidelines, variant-drug associations, and drug label data across two complementary endpoints. Search by gene symbol, drug name, or variant ID to retrieve clinical evidence levels, genotype-specific recommendations, and precision-medicine prescribing guidance."},"gist":{"api_url":"https://skillfed.io/api/skills/jaechang-hits/SciAgent-Skills/clinpgx-database.json","as_of":"2026-07-24","description":"Clinpgx Database queries pharmacogenomic clinical annotations and CPIC dosing guidelines for drug-gene.","install":{"manual":["git clone https://github.com/jaechang-hits/SciAgent-Skills","cp -r SciAgent-Skills ~/.claude/skills/clinpgx-database"],"primary":"npx skillfed install jaechang-hits/SciAgent-Skills/clinpgx-database","version":"42bdd667"},"kind":"skill","mirror_url":"https://skillfed.io/jaechang-hits/SciAgent-Skills/clinpgx-database.md","similar":[{"id":"synthetic-sciences/openscience/clinpgx-database","name":"clinpgx-database","publisher":"synthetic-sciences/openscience","url":"https://skillfed.io/synthetic-sciences/openscience/clinpgx-database"},{"id":"mims-harvard/ToolUniverse/tooluniverse-pharmacogenomics","name":"tooluniverse-pharmacogenomics","publisher":"mims-harvard/ToolUniverse","url":"https://skillfed.io/mims-harvard/ToolUniverse/tooluniverse-pharmacogenomics"}],"title":"Clinpgx Database by jaechang-hits \u2014 SkillFed","use":{"when":["ClinPGx Database offers two complementary endpoints to access clinical pharmacogenomics data.","Yes."]},"what":{"lead":"Clinpgx Database queries pharmacogenomic clinical annotations and CPIC dosing guidelines for drug-gene interactions.","rest":"ClinPGx Database provides REST API access to pharmacogenomic annotations, CPIC and DPWG dosing guidelines, variant-drug associations, and drug label data across two complementary endpoints. Search by gene symbol, drug name, or variant ID to retrieve clinical evidence levels, genotype-specific recommendations, and precision-medicine prescribing guidance."}},"id":"jaechang-hits/SciAgent-Skills/clinpgx-database","install":{"mode":"external","repo":"https://github.com/jaechang-hits/SciAgent-Skills"},"links":{"html":"https://skillfed.io/jaechang-hits/SciAgent-Skills/clinpgx-database","md":"https://skillfed.io/jaechang-hits/SciAgent-Skills/clinpgx-database.md","repo":"https://github.com/jaechang-hits/SciAgent-Skills"},"meta":{"agents_supported":[],"first_seen":"2026-07-28","forks":26,"language":"Python","last_updated":"2026-07-24","license":"NOASSERTION","name":"Clinpgx Database","publisher":"jaechang-hits","stars":284},"relations":{"similar":[{"id":"drshailesh88/integrated_content_OS/clinpgx-database"},{"id":"synthetic-sciences/openscience/clinpgx-database"},{"id":"LeonChaoX/qinyan-academic-skills/clinpgx-database"},{"id":"foryourhealth111-pixel/Vibe-Skills/clinpgx-database"},{"id":"mims-harvard/ToolUniverse/tooluniverse-pharmacogenomics"},{"id":"mims-harvard/ToolUniverse/tooluniverse-drug-mechanism-research"},{"id":"mims-harvard/ToolUniverse/tooluniverse-precision-medicine-stratification"},{"id":"jaechang-hits/SciAgent-Skills/ddinter-database"},{"id":"mims-harvard/ToolUniverse/tooluniverse-clinical-data-integration"},{"id":"jaechang-hits/SciAgent-Skills/kegg-database"}]},"slug":{"owner":"jaechang-hits","repo":"SciAgent-Skills","skill":"clinpgx-database"},"version":"42bdd667"}