We demonstrate the utility of this protocol in the context of an expanded, multi-cohort study, including APS1, patients with immune dysregulation, polyendocrinopathy, X-linked (IPEX), RAG1/2 deficiency with autoimmune features, a KD patient cohort, and emerging COVID-19 patient phenotypes with possible autoimmune underpinnings. This evidence concerns the gene RAG1 and COVID-19.