Tooluniverse Gwas Snp Interpretation

Pulls together GWAS Catalog and Open Targets data to answer "what does this SNP actually do" without you having to check five databases manually. You throw in an rsID like rs7903146, and it returns trait associations, fine-mapping credible sets, L2G gene predictions, and a clinical summary. The real value is that it understands a GWAS hit is a region, not a causal variant, so it checks LD structure and uses SuSiE/FINEMAP evidence before claiming mechanism. Takes 10 to 30 seconds for a full run. Most useful when you need to triage variants from a GWAS or explain why a lead SNP might regulate a gene 500kb away through an enhancer instead of the nearest gene.