Variant | Allele/Genotype | CON | Cases | O.R.(95%C.I.) | P-value |
---|---|---|---|---|---|
Hypertension |  | N = 1596 | N = 3521 |  |  |
rs2067853G > A | G | 0.681 | 0.711 | 1.15(1.04-1.28) | 0.007* |
 | GG | 0.870 | 0.906 | 1.44(1.17-1.78) | 0.001** |
rs7079G > T | G | 0.683 | 0.712 | 1.14(1.03-1.27) | 0.012 |
 | GG | 0.879 | 0.915 | 1.49(1.20-1.85) | <0.0001** |
rs699G > A | G | 0.560 | 0.602 | 1.19(1.08-1.31) | <0.0001** |
(p.M268T) | GG | 0.791 | 0.821 | 1.21(1.03-1.44) | 0.024 |
 | AG + GG | 0.328 | 0.383 | 1.26(1.10-1.46) | 0.001** |
rs3789679G > A | A | 0.028 | 0.042 | 1.51(1.14-1.99) | 0.004* |
AA | 0.005 | 0.012 | 2.70(1.07-6.83) | 0.036 | |
GA + AA | 0.052 | 0.072 | 1.41(1.05-1.90) | 0.022 | |
rs2148582G > A | G | 0.563 | 0.587 | 1.10(1.00-1.21) | 0.051 |
GG | 0.786 | 0.828 | 1.31(1.11-1.55) | 0.002* | |
rs5051T > C | C | 0.571 | 0.599 | 1.12(1.02-1.24) | 0.02 |
 | TC + CC | 0.800 | 0.843 | 1.32(1.13-1.60) | 0.001** |
Myocardial infarction |  | N = 1584 | N = 3033 |  |  |
rs2067853G > A | GG | 0.889 | 0.902 | 1.16(1.01-1.33) | 0.042 |
rs7079G > T | GG | 0.898 | 0.911 | 1.15(1.00-1.33) | 0.054 |
rs1926723T > C | T | 0.961 | 0.969 | 1.25(0.99-1.57) | 0.063 |
rs699G > A | G | 0.573 | 0.602 | 1.13(1.03-1.23) | 0.007* |
GG | 0.803 | 0.820 | 1.20(1.00-1.25) | 0.047 | |
AG + GG | 0.343 | 0.384 | 1.20(1.09-1.31) | <0.0001** | |
rs5051T > C | TC + CC | 0.822 | 0.838 | 1.12(1.00-1.25) | 0.051 |
Obesity |  | N = 3342 | N = 1721 |  |  |
rs4762G > A | G | 0.887 | 0.903 | 1.19(1.03-1.37) | 0.019 |
(p.M207T) | AG + GG | 0.192 | 0.167 | 0.85(0.72-0.99) | 0.040 |
rs3789679G > A | A | 0.032 | 0.050 | 1.59(1.28-1.98) | <0.0001** |
AA | 0.008 | 0.015 | 2.00(1.12-3.58) | 0.019 | |
 | GA + AA | 0.056 | 0.085 | 1.57(1.24-2.00) | <0.0001** |