Fig. 3From: Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorderAssociation of OXTR markers with narrow autism diagnosis in the AGRE sample. Markers are numbered as in Fig. 1. The OXTR intron 3 marker rs2268493 (marker 12) T allele was associated with narrow autism diagnosis using the recessive model (P = 0.043). The 3′ UTR marker rs1042778 G allele (marker 20) was associated with narrow autism using the recessive model (P = 0.041). The intergenic marker rs7632287 (marker 23) G allele was associated with narrow autism diagnosis using both the recessive model (P = 0.004) and the additive model (P = 0.031)Back to article page