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Frequency of intron B Bcl1, rs2307674 and rs6198 GR SNP genotypes in control and RA cases
| GR polymorphism | Controls n (%) | RA cases n (%) | P-value |
|---|---|---|---|
| Intron B BCl1 | (n = 392) | (n = 195) | |
| CC | 147 (37·5) | 76 (39·0) | |
| CG | 195 (49·7) | 94 (48·2) | |
| GG | 50 (12·8) | 25 (12·8) | 0·81 |
| (n = 384) | (n = 191) | ||
| rs2307674 | |||
| ttg/ttg | 255 (66·4) | 136 (71·2) | |
| ttg/- | 119 (31·0) | 47 (24·6) | |
| -/- | 10 (2·6) | 8 (4·2) | 0·50 |
| (n = 390) | (n = 178) | ||
| rs6198 | |||
| AA | 256 (65·6) | 129 (72·5) | |
| AG | 121 (31·1) | 44 (24·7) | |
| GG | 13 (3·3) | 5 (2·8) | 0·13 |
