Figure 1 — Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease

Research Paper|Volume 12, Issue 5|pp. 4379–4393

Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease

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100%

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.