Haplotype | F5: c.1601G > A | F5: c.6665A > G | Cases | Control | Total frequency | OR (95%CI) | p-value | P* |
1. | G | A | 0.928 | 0.876 | 0.902 | 1.00 | – | – |
2. | G | G | 0.056 | 0.120 | 0.088 | 0.35 (0.17–0.72) | 0.0048 | 0.0144 |
3. | A | G | 0.016 | 0.004 | 0.01 | 7.05 (0.72–69.36) | 0.095 | 0.142 |
4. | A | A | – | – | – | – | – | – |
Global haplotype association p-value: 0.0045 | Â | |||||||
Linkage disequilibrium analysis: D’ = 0.991, r2 = 0.091; p-value < 0.001 |  | |||||||
Haplotype | MTHFR: c.665C > T | MTHFR: c.1286A > C |  |  |  |  |  |  |
1. | C | A | 0.672 | 0.528 | 0.6 | 1.00 | – | – |
2. | C | C | 0.224 | 0.432 | 0.328 | 0.32 (0.21–0.51) | < 0.0001 | 0.0006 |
3. | T | C | 0.104 | 0.04 | 0.072 | 2.85 (1.29–6.29) | 0.0099 | 0.0198 |
4. | T | A | – | – | – | – | – | – |
Global haplotype association p-value< 0.0001 |  | |||||||
Linkage disequilibrium analysis: D’ = 0.999, r2 = 0.116; p-value < 0.001 |  | |||||||
Haplotype | VEGFA: c.*237C > T | VEGFA: c.-2055A > C |  |  |  |  |  |  |
1. | C | C | 0.552 | 0.54 | 0.546 | 1.00 | – | – |
2. | C | A | 0.364 | 0.348 | 0.356 | 1.26 (0.73–2.17) | 0.41 | 0.41 |
3. | T | A | 0.084 | 0.112 | 0.098 | 0.66 (0.34–1.25) | 0.20 | 0.24 |
4. | T | C | – | – | – | – | – |  |
Global haplotype association p-value: 0.38 | Â | |||||||
Linkage disequilibrium analysis: D’ = 0.9987, r2 = 0.13; p-value < 0.001, Bold fonts indicate significant P-value |  |