Skip to main content

Table 1 List of pathogenic or likely pathogenic variants in this study

From: Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders

  1. Chr chromosome, Ref reference allele, Alt alternate allele, De novo parents available to confirm de novo status, UAE United Arab Emirates, SA Saudi Arabia. Table includes individual variants from 4351 unrelated patients. Pathogenic variants are shaded in gray and likely pathogenic variants are unshaded