Table 2.
The genotypes and allele frequencies of FcγRIIB (rs1050501) and FcγRIIIA (rs396991) SNPs in patient and control groups
| Positions | Genotype and allele frequencies | Patients | Controls | OR (95% CI) | P value |
|---|---|---|---|---|---|
| 2n = 160 | 2n = 190 | ||||
| Rs1050501 | CC | 25 (31.25%) | 28 (29.47%) | 0.64 | |
| CT | 30 (37.5%) | 36 (37.89%) | |||
| TT | 75 (46.8%) | 31 (32.63%) | |||
| C | 85 (53.2%) | 92 (48.43%) | 0.93 (0.61–1.43) | 0.77 | |
| T | 38 (47.5%) | 98 (51.57%) | |||
| Rs396991 | TT | 25 (31.25%) | 42 (44.21%) | 0.73 | |
| TG | 17 (21.25%) | 35 (36.84%) | |||
| GG | 101 (63.1%) | 18 (18.94%) | |||
| T | 59 (36.9%) | 119 (62.63%) | 1.02 (0.66–1.57) | 0.92 | |
| G | 25 (31.25%) | 71 (37.36%) |
Values are indicated as count (percent)
The significance level was considered as P < 0.05