{"name":"broadinstitute-variant-interpreter-plugins-variant-interpreter","owner":{"name":"ClaudePluginHub"},"plugins":[{"name":"broadinstitute-variant-interpreter-plugins-variant-interpreter","source":{"source":"github","repo":"broadinstitute/tgg-llm-plugins"},"description":"Interpret variant pathogenicity from gnomAD CSV exports using ACMG/AMP guidelines, population frequency thresholds, and in silico prediction consensus","version":"1.0.0","strict":true,"keywords":["genomics","variant-interpretation","gnomad","pathogenicity","acmg","mendelian","csv"],"category":"deployment"}]}