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. 2014 Jan 23;9(1):e86007. doi: 10.1371/journal.pone.0086007

Table 3. Genotype frequencies in HBV carriers, resolved HBV and uninfected subjects in Thailand.

HBV carriers vs. Resolved HBV carriers vs. Uninfected
SNP Genotype HBV carriersa (n = 449) Resolved (n = 113) Uninfected (n = 123) OR (95% CI) P values OR (95% CI) P values
rs3077 CC 259 (57.7%) 43 (38.1%) 57 (46.3%) 1.00 - 1.00 -
HLA-DPA1 CT 153 (34.1%) 56 (49.6%) 46 (37.4%) 0.45 (0.29–0.71) <0.001 0.73 (0.47–1.13) 0.161
TT 37 (8.2%) 14 (12.4%) 20 (16.3%) 0.44 (0.22–0.88) 0.018 0.41 (0.22–0.75) 0.003
Dominant b 0.45 (0.30–0.69) <0.001 0.63 (0.42–0.95) 0.025
HWEp 0.038 0.516 0.049
rs9277378 GG 242 (53.9%) 40 (35.4%) 48 (39.0%) 1.00 - 1.00 -
HLA-DPB1 AG 177 (39.4%) 61 (54.0%) 54 (43.9%) 0.48 (0.31–0.75) 0.001 0.65 (0.42–1.00) 0.051
AA 30 (6.7%) 12 (10.6%) 21 (17.1%) 0.41 (0.20–0.87) 0.018 0.28 (0.15–0.54) <0.001
Dominant 0.47 (0.31–0.72) <0.001 0.55 (0.36–0.82) 0.003
HWEp 0.757 0.110 0.390
rs3128917 TT 99 (22.0%) 29 (25.7%) 38 (30.9%) 1.00 - 1.00 -
HLA-DPB1 TG 241 (53.7%) 60 (53.1%) 48 (39.0%) 1.18 (0.71–1.94) 0.525 1.93 (1.19–3.13) 0.008
GG 109 (24.3%) 24 (21.2%) 37 (30.1%) 1.33 (0.73–2.44) 0.355 1.13 (0.67–1.92) 0.648
Dominant 1.22 (0.76–1.97) 0.413 1.58 (1.02–2.46) 0.042
HWEp 0.117 0.496 0.015
rs1419881 TT 162 (36.1%) 31 (27.4%) 30 (24.4%) 1.00 - 1.00 -
TCF19 TC 213 (47.4%) 61 (54.0%) 60 (48.8%) 0.67 (0.41–1.08) 0.097 0.66 (0.41–1.07) 0.088
CC 74 (16.5%) 21 (18.6%) 33 (26.8%) 0.67 (0.36–1.25) 0.210 0.42 (0.24–0.73) 0.002
Dominant 0.67 (0.42–1.06) 0.084 0.57 (0.36–0.90) 0.015
HWEp 0.778 0.349 0.792
rs652888 TT 169 (37.6%) 50 (44.2%) 57 (46.3%) 1.00 - 1.00 -
EHMT2 TC 231 (51.4%) 50 (44.2%) 48 (39.0%) 1.37 (0.88–2.12) 0.162 1.62 (1.05–2.50) 0.027
CC 49 (10.9%) 13 (11.5%) 18 (14.6%) 1.12 (0.56–2.22) 0.756 0.92 (0.49–1.70) <0.001
Dominant 1.31 (0.87–2.00) 0.198 1.09 (0.65–1.82) 0.080
HWEp 0.022 0.926 0.142

Abbreviation: CI, confidence interval; OR, odds ratio ; HWEp, Hardy-Weinberg equilibrium analysis.

a

Defined as the combination between HCC and CHB.

b

Defined as a minor dominant according to the comparison between heterozygous+minor homozygous genotype and major homozygous genotype (eg. rs3077; CT+TT vs. CC).