{"slug":"tooluniverse-gwas-snp-interpretation","source_name":"tooluniverse-gwas-snp-interpretation","name":"Tooluniverse Gwas Snp Interpretation","description":"Interpret genetic variants (SNPs) from GWAS studies by aggregating evidence from multiple databases (GWAS Catalog, Open Targets Genetics, ClinVar). Retrieves variant annotations, GWAS trait associations, fine-mapping evidence, locus-to-gene predictions, and clinical significance. Use when asked to interpret a SNP by rsID, find disease associations for a variant, assess clinical significance, or answer questions like \"What diseases is rs429358 associated with?\" or \"Interpret rs7903146\".","version":1,"lift":{"pass_rate_delta_pts":31.82,"pass_rate_pct":31.8,"total_cases":22,"passed_cases":7,"tokens_delta_pct":79.3,"turns_delta_pct":0,"verdict":"mixed","benchmark_model":"gemini-3.6-flash","grading_method":"judged","completed_at":"2026-07-26T13:47:01.592064+00:00"},"skill_score":0.3182,"benchmark_models":[{"model":"gemini-3.6-flash","headline":true,"delta_pts":31.82,"with_pass_pct":31.8,"without_pass_pct":0,"tokens_delta_pct":79.3,"turns_delta_pct":0,"total_cases":22,"cases_aggregated":19,"verdict":"mixed","never_hurt":false,"completed_at":"2026-07-26T13:47:01.592064+00:00","run_id":"370e81a9-501a-4359-aea8-65329de251ba","version_number":1,"is_latest_version":true,"gate":null}],"trust":{"skill_safety":"passed","safety_status":"clean","intent_verdict":null,"content_status":"clean","indexable":true},"license":null,"install_count":0,"manifest_hash":"c27405e8befdf58c405afe31765adc64d634e04a33800fabaabe4f3f6c119481","raw_url":"https://app.decimal.ai/s/tooluniverse-gwas-snp-interpretation/SKILL.md","scorecard_url":"https://app.decimal.ai/skills/tooluniverse-gwas-snp-interpretation"}