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| marker | chromosome | gene | region | Allele (frequency) | Informative families | P-value |
| rs946252 | X | AMELX | Intron 2 | C/T (0.63/0.37) | 25 | 0.0007 |
| rs4970957 | 1 | TUFT1 | Intron 1 | A/G (0.55/0.45) | 36 | 0.67 |
| rs4694075 | 4 | AMBN | Intron 5 | C/T (0.32/0.68) | 35 | 0.20 |
| rs12640848 | 4 | ENAM | Intron 8 | A/G (0.80/0.20) | 24 | 0.38 |
| rs5997096 | 22 | TFIP11 | Intron 7 | C/T (0.43/0.57) | 37 | 0.46 |
Statistically significant p-values (p<0.05) are presented in bold font.
