Whole-exome sequencing identifies new pathogenic germline variants in patients with colorectal polyposis

Figure 1 Representative plot of variants identified in patients with polyposis. All genes harboring pathogenic (V) or likely pathogenic (IV) variants are shown (genes at the top). Genes harboring only variants of uncertain significance are shown if they have an indel, nonsense, or missense variant with a high pathogenic score (high variants of uncertain significance). ACMG: American College of Medical Genetics and Genomics.