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Table 4 The association of genotypes in RETN genes with the clinical phenotypes

From: Variants in RETN gene are associated with steroid-induced osteonecrosis of the femoral head risk among Han Chinese people

SNPGenotypeGenderpHip lesionspClinical stagesp
MaleFemaleUnilateralBilateralStage IIStage IIIStage IV
rs7408174CC860.775590.2853560.694
CT42351859193919
TT64433671245033
rs34861192AA010.465010.5470100.193
AG2923183415289
GG866041105326549
rs34124816AA94770.105511200.6504178520.557
CA2068186146
CC1102020
rs3219175AA010.470010.5920100.216
AG2822173315269
GG866041105316649
rs3745367AA1290.7753180.26331440.049*
AG48392760244419
GG55362962203635
rs3745368AA110.308020.6500200.613
AG2813122992111
GG867047109387147
rs3745369CC860.8764100.05921110.161
CG50402070204129
GG54373556244126
rs1477341AA2480.0639230.80962150.090
AT48422565214326
TT35332246172526
  1. p values were calculated by logistic regression
  2. Italicized value is statistically significant
  3. *p < 0.05 indicates statistical significance