Individual skill

tooluniverse-gwas-snp-interpretation

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".

skills/tooluniverse-gwas-snp-interpretation/SKILL.md

Source commit b1f9b6e3306f8d870e23b2023057bf730090036f

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Yes

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No

Observed behavior

Network or broad shell

Last checked

Nov 9, 2026

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