Table 4

DAS28 response data by genotype and association p values for three successfully genotyped SNPs in 1334 individuals

First and additional cohorts combined (n=1334)
Additive modelDominant model
SNPGeneChrbpGenotypeCountMean baseline DAS28SD baseline DAS28Mean change in DAS28SD change in DAS28HWE exact p valueGenotypic global p valueGlobal p valueCoefMin 95Max 95Global p valueCoefMin 95Max 95
rs10865035AFF32100202166AA3206.661.01−2.301.510.2280.0360.015−0.14−0.25−0.030.013−0.23−0.41−0.05
AG6886.650.97−2.511.49
GG3236.660.98−2.591.57
rs7574865STAT42191672878GG7386.690.97−2.561.510.4690.1730.2030.08−0.040.210.0910.13−0.020.29
GT5146.640.98−2.381.56
TT806.501.08−2.421.36
rs763361CD2261865682622TT3596.621.01−2.601.440.6220.1410.0480.110.000.220.0980.15−0.030.32
TC6576.650.95−2.481.56
CC3186.691.03−2.361.51
  • Significant p values (<0.05) are shown in bold type, italic indicates p<0.10.

  • bp, base pairs; Chr, chromosome; Coef, coefficient for minor allele (except at rs10865035); DAS, disease activity score; HWE, Hardy–Weinberg equilibrium; SNP, single nucleotide polymorphism.