Table 2.
Results of the association analysis
| SNP | p‐Value | FDR | Beta | Gene |
|---|---|---|---|---|
| rs17819126 | .0037 | 0.05 | 3.0 | DYX1C1 |
| rs8053211a | .0039 | 0.05 | −1.8 | ATP2C2 |
| rs2875891a | .0146 | 0.11 | −1.5 | ATP2C2 |
| rs3743204a | .0157 | 0.11 | −1.7 | DYX1C1 |
| rs16973771a | .0199 | 0.11 | −1.4 | ATP2C2 |
| rs11100040b | .0306 | 0.14 | 1.6 | Intergenic |
a
Denotes SNPs with lower p‐values as expected from multiple testing. For details see the QQ‐plot shown in Figure 2.
Five independent SNPs previously reported to be associated with dyslexia or dyslexia‐related phenotypes in at least two studies revealed a nominal association with the late component of MMR. Furthermore, one SNP previously reported to be associated with MMR was successfully replicated in our study (b). The p‐values of the regression model are shown with the respective FDR. Effect size Beta corresponds to carriage of the previously reported risk allele in the literature.