Among these were fgfr3 (fibroblast growth factor receptor 3, −0.45, adj p-value 0.00), which is involved in bone formation [42,43]; fbn2b (fibrillin 2b, −0.35, adj p-value 0.03), which is a candidate gene for Marfan syndrome and scoliosis in humans [11,44,45,46]; nav1 (neuron navigator 1, −0.39, adj p-value 0.03 [47]); dusp1 (dual specificity phosphatase 1, −0.37, adj p-value 0.04); prdx1 (peroxiredoxin 1, −0.36, adj p-value 0.01); and ranbp1 (RAN binding protein 1, −0.21, adj p-value 0.03 [48,49]. This evidence concerns the gene PRDX1 and scoliosis.