Table 3. Allele frequency and percentage across AML patients and controls.
| SNP ID | |||
|---|---|---|---|
| rs1799930 | Cases N (%) | Controls N (%) | p-value |
| Allele G | 46(79) | 292(67) | 0.058 |
| Allele A | 12(21) | 144(33) | |
| NA | 2 | 14 | |
| Genotype A/A | 3(10) | 21(10) | 0.023 |
| Genotype G/A | 6(21) | 102(47) | |
| Genotype G/G | 20(69) | 95(44) | |
| NA | 1 | 7 | |
| rs1799931 | |||
| Allele G | 53(95) | 383(98) | 0.119** |
| Allele A | 3(5) | 7(2) | |
| NA | 4 | 60 | |
| Genotype G/A | 3(11) | 7(4) | 0.116 |
| Genotype G/G | 25(89) | 188(96) | |
| NA | 2 | 30 | |
| rs121913500 | |||
| Allele C | 60(100) | 450(100) | ---- |
| rs121913502 | |||
| Allele C | 59(98) | 450(100) | 0.118** |
| Allele T | 1(2) | 0 | |
| Genotype C/C | 29(97) | 225(100) | 0.105** |
| Genotype C/T | 1(3) | 0 | |
| rs1057519736 | |||
| Allele G | 60(100) | 444(100) | ---- |
| NA | 0 | 6 |
** P-value retrieved from Fisher’s Exact Test in case cell count is less than 5 where Chi-square is not valid