ADNP and autism: The prevalence of indicative autism was variable across the 30 rare variant genotypes, being highest in individuals with ADNP variants (85%, OR in comparison to controls = 489.8, CI = 80.08–2995.41, p < 0.001 (mixed effects logistic regression)) and lowest in individuals with 22q11.2 deletion (10%, OR in comparison to controls = 4.2, CI = 1.94–9.02, p = 0.042 (mixed effects logistic regression)) (Fig. 1a, Supplementary Table S4).