A second pattern that emerged was the absence of clonal second “hits” (i.e. driver events) in recessive predisposition genes with an unclear link to Wilms tumour (NBN, PMS2, BLM (PD49219 only), BRCA2, CHEK2), consistent with the aforementioned lack of somatic mutational imprints of the underlying predisposition. The gene discussed is CHEK2; the disease is Wilms tumor.