Fig. 2From: Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorderAssociation of OXTR markers with ASD diagnosis in the entire sample of 1,238 families. Markers are numbered as in Fig. 1. The 3′ UTR marker rs1042778 G allele (marker 20) is associated with ASD diagnosis by the recessive model (P = 0.037). The intergenic marker rs7632287 (marker 23) G allele is associated with ASD diagnosis by both the recessive model (P = 0.016) and the additive model (P = 0.016)Back to article page