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Table 2 Genotype and allele distributions in patients with CAD and control subjects (Han population)

From: RETRACTED ARTICLE: A novel polymorphism of the GP78 gene is associated with coronary artery disease in Han population in China

 

Total

Men

Women

 

CAD n (%)

Control n (%)

P value

CAD n (%)

Control n (%)

P value

CAD n (%)

Control n (%)

P value

rs731119 (SNP1)

Genotype

 

G/G

369 (60.8)

375 (64.1)

0.236

237 (61.2)

227 (63.9)

0.695

132 (60)

148 (64.3)

0.283

A/A

21 (3.5)

26 (4.4)

11 (2.8)

11 (3.1)

10 (4.5)

15 (6.5)

A/G

217 (35.7)

184 (31.5)

139 (35.9)

117 (33)

78 (35.5)

67 (29.1)

 

Dominant model

GG

369 (60.8)

375 (64.1)

0.238

237 (61.2)

227 (63.9)

0.447

132 (60)

148 (64.3)

0.342

AG + AA

238 (39.2)

210 (35.9)

150 (38.8)

128 (36.1)

88 (40)

82 (35.7)

Recessive model

AA

21 (3.5)

26 (4.4)

0.382

11 (2.8)

11 (3.1)

0.837

10 (4.5)

15 (6.5)

0.36

AG + GG

572 (99.83)

455 (100)

376 (97.2)

344 (96.9)

210 (95.5)

215 (93.5)

Additive model

AG

217 (35.7)

184 (31.5)

0.117

139 (35.9)

117 (33)

0.447

78 (35.5)

67 (29.1)

0.342

GG + AA

390 (64.3)

401 (68.5)

237 (61.2)

227 (63.9)

132 (60)

148 (64.3)

Allele

 

G

955 (78.7)

934 (79.8)

0.484

613 (79.2)

571 (80.4)

0.558

342 (77.7)

363 (78.9)

0.666

A

259 (21.3)

236 (20.2)

161 (20.8)

139 (19.6)

98 (22.3)

97 (21.1)

rs2617849 (SNP2)

Genotype

 

T/T

222 (39.9)

181 (38.8)

0.046

132 (37.8)

102 (31.1)

0.159

90 (43.3)

79 (35.3)

0.234

C/C

74 (13.3)

87 (15.8)

49 (14)

56 (17.1)

25 (12)

31 (13.8)

C/T

261 (46.9)

284 (51.4)

168 (48.1)

170 (51.8)

93 (44.7)

114 (50.9)

 

Dominant model

TT

222 (39.9)

181 (38.8)

0.014*

132 (37.8)

102 (31.1)

0.066

90 (43.3)

79 (35.3)

0.89

CC + CT

335 (60.1)

371 (67.2)

217 (62.2)

226 (68.9)

118 (56.7)

145 (64.7)

Recessive model

CC

74 (13.3)

87 (15.8)

0.242

49 (51.9)

56 (17.1)

0.276

25 (12)

31 (13.8)

0.574

TT + CT

483 (86.7)

465 (84.2)

300 (86)

272 (82.9)

183 (88)

193 (86.2)

Additive model

CT

261 (46.9)

284 (51.4)

0.126

168 (48.1)

170 (51.8)

0.337

93 (44.7)

114 (50.9)

0.199

CC + TT

296 (53.1)

268 (48.6)

181 (51.9)

158 (48.2)

115 (55.3)

110 (49.1)

Allele

 

C

409 (37.7)

458 (41.5)

0.021*

266 (38.1)

282 (43)

0.068

143 (34.4)

176 (39.3)

0.135

T

705 (63.3)

646 (58.5)

432 (61.9)

374 (57)

273 (65.6)

272 (60.7)

rs2440472 (SNP3)

Genotype

 

A/A

164 (27.2)

187 (32.7)

0.008*

110 (28.4)

123 (36.1)

0.007*

54 (25.2)

64 (27.7)

0.582

G/G

144 (23.9)

98 (17.1)

95 (24.5)

54 (15.8)

49 (22.9)

44 (19)

A/G

294 (48.8)

287 (50.2)

183 (47.2)

164 (48.1)

111 (51.9)

123 (53.2)

 

Dominant model

A/A

164 (27.2)

187 (32.7)

0.041*

110 (28.4)

123 (36.1)

0.026*

54 (25.2)

64 (27.7)

0.555

GG + AG

438 (72.8)

385 (67.3)

278 (71.6)

218 (63.9)

160 (74.8)

167 (72.3)

Recessive model

GG

144 (23.9)

98 (17.1)

0.004*

95 (24.5)

54 (15.8)

0.004*

49 (22.9)

44 (19)

0.318

AA + AG

458 (76.1)

474 (82.9)

293 (75.5)

287 (84.2)

165 (77.1)

187 (81)

Additive model

AG

294 (48.8)

287 (50.2)

0.647

183 (47.2)

164 (48.1)

0.802

111 (51.9)

123 (53.2)

0.771

AA + GG

308 (51.2)

285 (49.8)

205 (52.8)

177 (51.9)

103 (48.1)

108 (46.8)

Allele

 

A

622 (51.7)

661 (57.8)

0.003*

403 (51.9)

410 (60.1)

0.002*

219 (51.2)

251 (54.3)

0.345

   

G

582 (48.3)

483 (42.2)

 

373 (48.1)

272 (39.9)

 

209 (48.8)

211 (45.7)

 
  1. CAD, coronary artery disease.
  2. The P value of genotype was calculated by Fisher’s exact test. *P<0.05.