NOP56 and cerebellar ataxia: Protein coding genes proximal to these snoRNAs were implicated in several neurologic conditions, including Wernicke‐Korsakoff Syndrome (Tex2/SNORD104), Spinocerebellar Ataxia (Nop56/SNORD57), and Parkinson Disease (EIF4A2/SNORD2; Table S5).