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. 2015 May 10;32(7):1123–1128. doi: 10.1007/s10815-015-0493-3

Table 2.

Distribution of HMGB1 SNPs in patients and controls

Polymorphisms Patients (N = 112) (%) Controls (N = 118) (%) OR (95% CI) P value Overall P value a
rs2249825 C/G
 Genotype 0.046*
 CC 55 (49.1) 72 (61.0) Ref.
 CG 25 (22.3) 28 (23.7) 1.17 (0.61–2.23) 0.635
 GG 32 (28.6) 18 (15.3) 2.33 (1.18–4.58) 0.013*
Allele
 C 135 (60.3) 172 (72.9) Ref.
 G 89 (39.7) 64 (27.1) 1.77 (1.20–2.62) 0.004*
rs1412125 T/C
 Genotype 0.905
 TT 62 (55.4) 66 (55.9) Ref.
 TC 40 (35.7) 41 (34.7) 1.04 (0.60–1.81) 0.894
 CC 10 (8.9) 11 (9.4) 0.97 (0.38–2.44) 0.945
Allele
 T 164 (73.2) 173 (73.3) Ref.
 C 60 (26.8) 63 (26.7) 1.01 (0.66–1.52) 0.983

*P value < 0.05. aOverall p-value across the three genotypes of a polymorphism