Table II.
Genotype and variant allele frequencies for FTO gene polymorphism rs8050136: A>C.
Polymorphism | Genotype | T2D patients | Mutated allele frequency | Prediabetic patients | Mutated allele frequency | Healthy controls | Mutated allele frequency | p |
---|---|---|---|---|---|---|---|---|
rs8050136 | AA | 130 (24.7%) | 0.50 | 17 (41.3%) | 0.46 | 84 (26.0%) | 0.51 | p preD/ctrl = 0.100 |
AC | 264 (50.1%) | 16 (30.4%) | 150 (46.4%) | p T2D/preD = 0.576 | ||||
CC | 133 (25.2%) | 13 (28.3%) | 89 (27.6%) | P preD/ctrl = 0.224 | ||||
Total | 527 | P1 =0.999 | 46 | P2=0.127 | 323 | P3=0.443 | p=0.258 |
p – significance of the 2 test for comparison of genotype frequencies between T2D, prediabetic patients and healthy controls ppreD/ctrl – significance of the 2 test for comparison of genotype frequencies between T2D and prediabetic patients p significance of the 2 test for comparison of genotype frequencies between T2D patients and healthy controls p T2D/preD – significance of the 2 test for comparison of genotype frequencies between prediabetic patients and healthy controls
P1 – value for Hardy-Weinberg equilibrium for T2D patients group
P2 – value for Hardy-Weinberg equilibrium for pre-diabetic patients group
P3 – value for Hardy-Weinberg equilibrium for healthy controls group