Table 5. Allele frequencies of MECP2 SNPs in European-derived SLE patients and controls.
SNP | Risk allele | Risk allele frequency* | Chi2 | OR (95% CI) | p value | Permutation p value | HWE (p value) | |||
Cases n (%) | Controls n (%) | Cases | Controls | |||||||
rs2266890 | A | 418 (21.2) | 354 (18.0) | 6.24 | 1.22 | (1.04–1.43) | 0.013 | 0.068 | 0.45 | 0.21 |
rs2075596 | A | 371(18.5) | 301(15.5) | 8.59 | 1.28 | (1.09–1.52) | 0.0034 | 0.02 | 0.70 | 1 |
rs3027933 | C | 383 (19.1) | 308 (15.3) | 9.83 | 1.30 | (1.10–1.53) | 0.0017 | 0.01 | 0.72 | 0.92 |
rs3027935 | G | 1879 (93.8) | 1865 (93.0) | 1.01 | 1.14 | (0.89–1.46) | 0.31 | 0.79 | 0.03 | 0.14 |
rs3027939 | G | 104 (5.5) | 97 (5.0) | 0.57 | 1.12 | (0.84–1.48) | 0.45 | 0.92 | 0.02 | 0.68 |
rs17435 | T | 500 (24.9) | 411 (20.5) | 11.25 | 1.29 | (1.11–1.49) | 0.0008 | 0.0047 | 0.27 | 0.36 |
rs1624766 | G | 497 (24.8) | 412 (20.5) | 10.39 | 1.28 | (1.10–1.48) | 0.0013 | 0.0074 | 0.48 | 0.36 |
rs7884370 | G | 109 (5.4) | 98 (4.9) | 0.63 | 1.12 | (0.85–1.48) | 0.43 | 0.91 | 0.02 | 0.68 |
rs1734787 | C | 387 (19.3) | 307 (15.3) | 11.15 | 1.32 | (1.12–1.56) | 0.0008 | 0.0048 | 1 | 0.92 |
rs5987201 | A | 109 (5.4) | 98 (4.9) | 0.62 | 1.12 | (0.85–1.48) | 0.43 | 0.91 | 0.02 | 0.68 |
rs1734791 | A | 389 (19.4) | 311 (15.5) | 10.43 | 1.31 | (1.11–1.54) | 0.0012 | 0.0072 | 0.91 | 1 |
rs1734792 | A | 388 (19.3) | 311 (15.5) | 10.27 | 1.31 | (1.11–1.54) | 0.0014 | 0.0078 | 0.88 | 1 |
rs11156611 | A | 108 (5.4) | 98 (4.9) | 0.51 | 1.11 | (0.84–1.47) | 0.47 | 0.94 | 0.02 | 0.68 |
rs2239464 | A | 475 (23.7) | 400 (19.9) | 8.13 | 1.24 | (1.07–1.45) | 0.0044 | 0.026 | 0.72 | 0.27 |
rs5945175 | G | 115 (5.7) | 103 (5.1) | 0.70 | 1.12 | (0.86–1.48) | 0.40 | 0.89 | 0.85 | 0.45 |
OR, odds ratio; CI, confidence interval; HWE, Hardy-Weinberg equilibrium.
A total of 1080 independent cases and 1080 healthy unrelated controls matched for race and sex were genotyped