In total, 12,785 variants were annotated to nine candidate genes previously implicated in dyslexia by at least two independent studies, namely DYX1C1, DCDC2, KIAA0319, C2ORF3, MRPL19, ROBO1, GRIN2B, FOXP2, and CNTNAP2. We reported associations for all these variants in Table S7a–h. The gene discussed is GCFC2; the disease is dyslexia.