Previous GWASs have discovered several inherited common variants in some chromosomal regions that are significantly associated with the risk of neuroblastoma, such as LINC00340 (also known as FLJ22536 or CASC15) at 6p22 [1], BARD1 at 2q35 [20], and LIM domain only 1 (LMO1) at 11p15 [21]. The gene discussed is LMO1; the disease is neuroblastoma.