{"enrichment":{"faq":[{"a":"Gwas Database provides access to the NHGRI-EBI GWAS Catalog REST API, enabling you to search published genome-wide association studies and retrieve SNP-trait associations, variants, and summary statistics. You can query by disease trait, PubMed ID, variant, or chromosomal region to explore genetic architecture and check pleiotropy without requiring authentication.","q":"What is Gwas Database and what can I search with it?"},{"a":"Gwas Database lets you query the GWAS Catalog by multiple parameters: search for specific traits or diseases, look up PubMed IDs to find associated studies, search individual SNPs or variants, or specify chromosomal regions. Each query returns comprehensive association data including effect sizes and p-values to support your genetic research.","q":"How do I perform a genome wide association studies lookup?"},{"a":"Yes, Gwas Database supports variant-focused searches through its gwas SNP search capability. You can look up specific SNPs to retrieve their associations with phenotypic traits, annotation details, and summary statistics across published studies in the GWAS Catalog.","q":"Can I find genetic variants and SNP information in Gwas Database?"},{"a":"Gwas Database aggregates population-level genetic association data from published genome-wide association studies, including SNP-trait associations, locus information, variant annotations, and summary statistics. This enables exploration of genetic architecture, pleiotropy assessment, and identification of candidates for polygenic risk score construction.","q":"What types of genetic association data does Gwas Database contain?"},{"a":"No, Gwas Database requires no authentication. You can freely access the NHGRI-EBI GWAS Catalog REST API to search and retrieve genome-wide association study results and genetic variant information for your research.","q":"Do I need authentication to access Gwas Database?"},{"a":"Gwas Database enables genetic trait association searches by querying the GWAS Catalog for specific phenotypes or diseases. You can explore which SNPs and genomic loci are associated with your trait of interest, review effect sizes and statistical significance, and build candidate lists for further validation or polygenic risk modeling.","q":"How can I use Gwas Database for genetic trait association searches?"}],"shadow_tags":["genomic-research","variant-discovery","statistical-genetics","trait-association","snp-annotation","population-genetics","biomedical-data","genetic-epidemiology"],"summary_rewrite":"Access the NHGRI-EBI GWAS Catalog REST API to search published genome-wide association studies and retrieve SNP-trait associations, variants, and summary statistics. Query by disease trait, PubMed ID, variant, or chromosomal region to explore genetic architecture, check pleiotropy, and build polygenic risk score candidates. No authentication required."},"gist":{"api_url":"https://skillfed.io/api/skills/jaechang-hits/SciAgent-Skills/gwas-database.json","as_of":"2026-07-24","description":"Gwas Database lets you search published genome-wide association studies and retrieve SNP-trait associations.","install":{"manual":["git clone https://github.com/jaechang-hits/SciAgent-Skills","cp -r SciAgent-Skills ~/.claude/skills/gwas-database"],"primary":"npx skillfed install jaechang-hits/SciAgent-Skills/gwas-database","version":"16f746a3"},"kind":"skill","mirror_url":"https://skillfed.io/jaechang-hits/SciAgent-Skills/gwas-database.md","similar":[{"id":"synthetic-sciences/openscience/gwas-database","name":"gwas-database","publisher":"synthetic-sciences/openscience","url":"https://skillfed.io/synthetic-sciences/openscience/gwas-database"},{"id":"mims-harvard/ToolUniverse/tooluniverse-gwas-trait-to-gene","name":"tooluniverse-gwas-trait-to-gene","publisher":"mims-harvard/ToolUniverse","url":"https://skillfed.io/mims-harvard/ToolUniverse/tooluniverse-gwas-trait-to-gene"},{"id":"mims-harvard/ToolUniverse/tooluniverse-regulatory-variant-analysis","name":"tooluniverse-regulatory-variant-analysis","publisher":"mims-harvard/ToolUniverse","url":"https://skillfed.io/mims-harvard/ToolUniverse/tooluniverse-regulatory-variant-analysis"},{"id":"mims-harvard/ToolUniverse/tooluniverse-population-genetics-1000genomes","name":"tooluniverse-population-genetics-1000genomes","publisher":"mims-harvard/ToolUniverse","url":"https://skillfed.io/mims-harvard/ToolUniverse/tooluniverse-population-genetics-1000genomes"},{"id":"mims-harvard/ToolUniverse/tooluniverse-gwas-study-explorer","name":"tooluniverse-gwas-study-explorer","publisher":"mims-harvard/ToolUniverse","url":"https://skillfed.io/mims-harvard/ToolUniverse/tooluniverse-gwas-study-explorer"}],"title":"Gwas Database by jaechang-hits \u2014 SkillFed","use":{"when":["Gwas Database lets you query the GWAS Catalog by multiple parameters: search for specific traits or diseases.","Yes, Gwas Database supports variant-focused searches through its gwas SNP search capability."]},"what":{"lead":"Gwas Database lets you search published genome-wide association studies and retrieve SNP-trait associations without authentication.","rest":"Access the NHGRI-EBI GWAS Catalog REST API to search published genome-wide association studies and retrieve SNP-trait associations, variants, and summary statistics. Query by disease trait, PubMed ID, variant, or chromosomal region to explore genetic architecture, check pleiotropy, and build polygenic risk score candidates. No authentication required."}},"id":"jaechang-hits/SciAgent-Skills/gwas-database","install":{"mode":"external","repo":"https://github.com/jaechang-hits/SciAgent-Skills"},"links":{"html":"https://skillfed.io/jaechang-hits/SciAgent-Skills/gwas-database","md":"https://skillfed.io/jaechang-hits/SciAgent-Skills/gwas-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":"Gwas Database","publisher":"jaechang-hits","stars":284},"relations":{"similar":[{"id":"synthetic-sciences/openscience/gwas-database"},{"id":"LeonChaoX/qinyan-academic-skills/gwas-database"},{"id":"drshailesh88/integrated_content_OS/gwas-database"},{"id":"mims-harvard/ToolUniverse/tooluniverse-gwas-trait-to-gene"},{"id":"mims-harvard/ToolUniverse/tooluniverse-polygenic-risk-score"},{"id":"mims-harvard/ToolUniverse/tooluniverse-regulatory-variant-analysis"},{"id":"mims-harvard/ToolUniverse/tooluniverse-population-genetics-1000genomes"},{"id":"mims-harvard/ToolUniverse/tooluniverse-gwas-snp-interpretation"},{"id":"mims-harvard/ToolUniverse/tooluniverse-gwas-study-explorer"},{"id":"synthetic-sciences/openscience/curated-bio-datasets"}]},"slug":{"owner":"jaechang-hits","repo":"SciAgent-Skills","skill":"gwas-database"},"version":"16f746a3"}