Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease
Figure 1.Assessment of linkage disequilibrium (LD) between the genetic variants within RET, ARHGEF3 and CTNNAL1. The matrices represent the D' value between the SNP pairs. Red matrices denote D' > 70%. SNP = single nucleotide polymorphism.