Skip to main content

Table 3 Genotype and allele distributions in patients with CAD and control subjects (Uygur 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From: RETRACTED ARTICLE: A novel polymorphism of the GP78 gene is associated with coronary artery disease in Han population in China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

269 (63)

244 (64.4)

0.811

202 (62.7)

146 (63.8)

0.873

67 (63.8)

98 (65.3)

0.968

A/A

18 (4.2)

18 (4.7)

12 (3.7)

10 (4.4)

6 (5.7)

8 (5.3)

A/G

140 (32.8)

117 (30.9)

108 (33.5)

73 (31.9)

32 (30.5)

44 (29.3)

 

Dominant model

GG

269 (63)

244 (64.4)

0.684

202 (62.7)

146 (63.8)

0.806

67 (63.8)

98 (65.3)

0.802

AG + AA

158 (37)

135 (35.6)

120 (37.3)

83 (36.2)

38 (36.2)

52 (34.7)

Recessive model

AA

18 (4.2)

18 (4.7)

0.714

12 (3.7)

10 (4.4)

0.705

6 (5.7)

8 (5.3)

0.895

AG + GG

409 (95.8)

361 (95.3)

310 (96.3)

219 (95.6)

99 (94.3)

142 (94.7)

Additive model

AG

140 (32.8)

117 (30.9)

0.56

108 (33.5)

73 (31.9)

0.682

32 (30.5)

44 (29.3)

0.844

GG + AA

287 (67.2)

262 (69.1)

214 (66.5)

156 (68.1)

73 (69.5)

106 (70.7)

Allele

 

G

678 (79.4)

605 (79.8)

0.833

512 (79.5)

365 (79.7)

0.938

166 (79)

240 (80)

0.793

A

176 (20.6)

153 (20.2)

132 (20.5)

93 (20.3)

44 (21)

60 (20)

rs2617849 (SNP2)

Genotype

 

T/T

152 (39.7)

128 (35.4)

0.576

120 (42.6)

78 (36.1)

0.346

32 (31.7)

50 (34.2)

0.869

C/C

57 (14.9)

58 (16)

36 (12.8)

31 (14.4)

21 (20.8)

27 (18.5)

C/T

174 (45.4)

176 (48.6)

126 (44.7)

107 (49.5)

48 (47.5)

69 (47.3)

 

Dominant model

TT

152 (39.7)

128 (35.4)

0.223

120 (42.6)

78 (36.1)

0.145

32 (31.7)

50 (34.2)

0.674

CC + CT

231 (60.3)

234 (64.6)

162 (57.4)

138 (63.9)

69 (68.3)

96 (65.8)

Recessive model

CC

57 (14.9)

58 (16)

0.667

36 (12.8)

31 (14.4)

0.607

21 (20.8)

27 (18.5)

0.653

TT + CT

326 (85.1)

304 (84)

246 (87.2)

185 (85.6)

80 (79.2)

119 (81.5)

Additive model

CT

174 (45.4)

176 (48.6)

0.384

126 (44.7)

107 (49.5)

0.282

48 (47.5)

69 (47.3)

0.967

CC + TT

209 (54.6)

186 (51.4)

156 (55.3)

109 (50.5)

53 (52.5)

77 (52.7)

Allele

 

C

288 (37.6)

292 (40.3)

0.279

198 (35.1)

169 (39.1)

0.193

90 (44.6)

123 (42.1)

0.592

T

478 (62.4)

432 (59.7)

366 (64.9)

263 (60.9)

112 (55.4)

169 (57.9)

rs2440472 (SNP3)

Genotype

 

A/A

85 (22.7)

78 (20.7)

0.269

57 (20.4)

43 (19.1)

0.316

28 (29.5)

35 (23.2)

0.513

G/G

120 (32.1)

106 (28.2)

94 (33.7)

64 (28.4)

26 (27.4)

42 (27.8)

A/G

169 (45.2)

192 (51.1)

128 (45.9)

118 (52.4)

41 (43.2)

74 (49)

 

Dominant model

A/A

85 (22.7)

78 (20.7)

0.51

57 (20.4)

43 (19.1)

o.712

28 (29.5)

35 (23.2)

0.271

GG + AG

289 (77.3)

298 (79.3)

222 (79.6)

182 (80.9)

67 (70.5)

116 (76.8)

Recessive model

GG

120 (32.1)

106 (28.2)

0.245

94 (33.7)

64 (28.4)

0.207

26 (27.4)

42 (27.8)

0.939

AA + AG

254 (67.9)

270 (71.8)

185 (66.3)

161 (71.6)

69 (72.6)

109 (72.2)

Additive model

AG

169 (45.2)

192 (51.1)

0.107

128 (45.9)

118 (52.4)

0.143

41 (43.2)

74 (49)

0.371

AA + GG

205 (54.8)

184 (48.9)

151 (54.1)

107 (47.6)

54 (56.8)

77 (51)

Allele

 

A

339 (45.3)

348 (46.3)

0.71

242 (43.4)

204 (45.3)

0.533

97 (51.1)

144 (47.7)

0.467

   

G

409 (54.7)

404 (53.7)

 

316 (56.6)

246 (54.7)

 

93 (48.9)

158 (52.3)

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