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. 2019 Jul 2;20(3):2177–2188. doi: 10.3892/mmr.2019.10455

Table V.

Genotype and allele frequencies of five SNPs of APOBEC3H.

A, Rs56695217 genotype and allele

CHB patients (n=104) LC patients (n=265) HCC patients (n=287)



SNP N (%) OR (95%Cl) P-valuea N (%) OR (95%Cl) P-valueb N (%) OR (95%Cl) P-valuec
Number detected n=89 n=235 n=241
CC 11 (12.4) 1 29 (12.3) 26 (10.8)
CG 76 (85.4) 1.03 (0.49,2.17) 0.94 203 (86.4) 1.26 (0.71,2.25) 0.43 214 (88.8) 1.17 (0.54,2.56) 0.69
GG 2 (2.2) 0.60 (0.09,4.13) 0.60 3 (1.3) 0.34 (0.03,3.64) 0.36 1 (0.4) 0.11 (0.01,1.37) 0.08
CG+GG 78 1.02 (0.48,2.15) 0.96 206 1.25 (0.70,2.22) 0.45 215 1.14 (0.53,2.47) 0.74
C Allele 98 (55.1) 1 261 (55.5) 1 266 (55.2) 1
G Allele 80 (44.9) 0.98 (0.69,1.39) 0.91 209 (44.5) 0.99 (0.76,1.27) 0.92 216 (44.8) 1.00 (0.71,1.42) 0.98

B, Rs139292 genotype and allele

CHB patients (n=104) LC patients (n=265) HCC patients (n=287)



SNP N (%) OR (95%Cl) P-valuea N (%) OR (95%Cl) P-valueb N (%) OR (95%Cl) P-valuec

Number detected n=95 n=247 n=250
DEL 42 (44.2) 1 111 (44.9) 1 112 (44.8) 1
CAA.DEL 53 (55.8) 0.97 (0.60,1.57) 0.90 134 (54.3) 1.04 (0.72,1.49) 0.84 137 (54.8) 1.03 (0.91,0.63) 0.91
CAA 0 (0.0) 0.73 (0.66,0.80) 1.00 2 (0.8) 0.50 (0.60,7.09) 0.68 1 (0.4) 0.73 (0.66,0.80) 1.00
DEL+CAA 53 0.99 (0.61,1.60) 0.95 136 1.03 (0.72,1.48) 0.86 138 1.03 (0.63,1.69) 0.89
DEL Allele 137 (72.1) 1 356 (72.1) 1 361 (72.2) 1
CAA Allele   53 (27.9) 0.69 (1.00,1.46) 1.00 138 (27.9) 0.99 (0.75,1.31) 1.00 139 (27.8) 0.99 (0.69,1.45) 1.00

C, Rs139297 genotype and allele

CHB patients (n=104) LC patients (n=265) HCC patients (n=287)



SNP N (%) OR (95%Cl) P-valuea N (%) OR (95%Cl) P-valueb N (%) OR (95%Cl) P-valuec

Number detected n=102 n=263 n=280
CC 41 (40.2) 1 115 (43.7) 1 118 (42.1) 1
CG 16 (15.7) 0.84 (0.42,1.68) 0.63 38 (14.4) 0.95 (056,1.62) 0.85 36 (12.9) 0.85 (0.42,1.72) 0.65
GG 45 (44.1) 0.87 (0.52,1.44) 0.58 110 (41.8) 1.78 (0.81,1.70) 0.39 126 (45.0) 1.07 (0.64,1.79) 0.79
CG+GG 61 0.86 (0.54,1.38) 0.53 143 1.12 (0.79,1.58) 0.53 174 1.01 (0.63,1.63) 0.97
C Allele 98 (49.4) 1 268 (49.8) 272 (77.0) 1
G Allele 106 (50.6) 0.89 (0.64,1.23) 0.48 258 (50.2) 1.15 (0.89,1.48) 0.28 288 (23.0) 0.98 (0.71,1.35) 0.90

D, Rs139302 genotype and allele

CHB patients (n=104) LC patients (n=265) HCC patients (n=287)



SNP N (%) OR (95%Cl) P-valuea N (%) OR (95%Cl) P-valueb N (%) OR (95%Cl) P-valuec

Number detected n=89 n=229 n=255
CC 34 (38.2) 1 86 (37.6) 1 81 (31.8) 1
CG 20 (22.5) 1.1 (0.57,2.11) 0.79 56 (24.5) 1.38 (0.86,2.20) 0.18 74 (29.0) 1.53 (0.80,2.94) 0.20
GG 35 (39.3) 0.98 (0.55,1.72) 0.93 87 (30.8) 1.25 (0.82,1.91) 0.30 100 (39.2) 1.31 (0.73,2.33) 0.37
CG+GG 55 1.02 (0.61,1.70) 0.94 143 1.30 (0.89,1.90) 0.18 174 1.39 (0.83,2.24) 0.21
C Allele 88 (49.4) 1 228 (49.8) 1 236 (46.3) 1
G Allele 90 (50.6) 0.99 (0.70,1.40) 0.94 230 (50.2) 0.87 (0.68,1.12) 0.28 274 (53.7) 0.88 (0.63,1.24) 0.47

E, Rs139316 genotype and allele

CHB patients (n=104) LC patients (n=265) HCC patients (n=287)



SNP N (%) OR (95%Cl) P-valuea N (%) OR (95%Cl) P-valueb N (%) OR (95%Cl) P-valuec

Number detected n=103 n=263 n=281
CC 17 (16.5) 1 43 (16.3) 1 37 (13.2) 1
CT 46 (44.7) 1.02 (0.52,1.97) 0.96 117 (44.5) 0.26 (0.75,2.10) 0.39 133 (47.3) 1.36 (0.69,2.69) 0.38
TT 40 (38.8) 1.01 (0.51,2.00) 0.97 103 (39.2) 1.24 (0.73,2.10) 0.42 111 (39.5) 1.40 (0.69,2.77) 0.37
CT+TT 86 1.01 (0.54,1.89) 0.97 220 1.25 (0.77,2.03) 0.37 244 1.37 (0.72,2.60) 0.34
C Allele 80 (38.3) 1 203 (38.6) 1 207 (36.8) 1
T Allele 126 (61.2) 1.01 (0.73,1.41) 0.95 323 (61.4) 0.93 (0.73,1.86) 0.55 355 (63.2) 1.09 (0.78,1.51) 0.61

The two-sided χ2 test or Fisher's exact test was used in the comparison of allele distributions.

a

CHB vs. LC

b

LC vs. HCC

c

CHB vs. HCC, adjusted for age, gender, smoking and alcohol consumption by logistic regression analysis. APOBEC3, apolipoprotein B mRNA-editing catalytic polypeptide-like 3; SNPs, single nucleotide polymorphisms; CHB, chronic hepatitis B; LC, liver cirrhosis; HCC, hepatocellular carcinoma; OR, odds ratio; CI, confidence intervals.

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