highly significantP =0.0005
Using the cohorts from PARIS and Canada and the ExAC data set, the enrichment of rare CNTN6 variants in individuals with ASD compared with the general population was highly significant (ASD: 18/501; 3.59% controls: 535/33 480; 1.6% P =0.0005) and with an achieved power to observe such a difference of 87%.