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Table 2 Detailed analysis for rs11102930, genotyped in 1120 and 869 controls.

From: Genomic NGFBvariation and multiple sclerosis in a case control study

       

Genotype (%)

p value

SNP

(maj./min. allele)

cohort

Stratif-ication

Maj. allele (%)

Min. allele (%)

p value

OR (CI*1)

XX

Xx

xx

Geno-type

Major allel dominant

co-dominant

Minor allele dominant

HWE p value

N

rs11102930 (T/C)

MS

Ø

1380 (64.3)

766 (35.7)

0.5414

0.959 (0.840–1.096)

449 (41.8)

482 (44.9)

142 (13.2)

0.6694

0.3713

0.7157

0.8148

0.48

1073

  

male

423 (60.8)

273 (39.2)

0.0115

0.765 (0.622–0.942)

124 (35.6)

175 (50.3)

49 (14.1)

0.0259

0.2272

0.0664

0.0075

0.31

348

  

female

957 (66.0)

493 (34.0)

0.2271

1.115 (0.934–1.332)

325 (44.8)

307 (42.3)

93 (12.8)

0.1682

0.8954

0.0695

0.0829

0.13

725

  

rr Ø

764 (65.1)

410 (34.9)

0.9120

0.991 (0.848–1.158)

251 (42.8)

262 (44.6)

74 (12.6)

0.8773

0.6845

0.7010

0.9061

0.66

587

  

rr male

212 (59.2)

146 (40.8)

0.0101

0.717 (0.557–0.924)

59 (33.0)

94 (52.5)

26 (14.5)

0.0206

0.2537

0.0465

0.0056

0.24

179

  

rr female

552 (67.6)

264 (32.4)

0.0760

1.201 (0.981–1.472)

192 (47.1)

168 (41.2)

48 (11.8)

0.0872

0.7263

0.0525

0.0295

0.23

408

  

sp Ø

303 (62.9)

179 (37.1)

0.3324

0.901 (0.731–1.112)

97 (40.2)

109 (45.2)

35 (14.5)

0.5288

0.2712

0.8855

0.5545

0.63

241

  

sp male

78 (59.1)

54 (40.9)

0.0764

0.714 (0.491–1.036)

23 (34.8)

32 (48.5)

11 (16.7)

0.2125

0.2026

0.4665

0.1183

0.98

66

  

sp female

225 (64.3)

125 (35.7)

0.7989

1.034 (0.798–1.341)

74 (42.3)

77 (44.0)

24 (13.7)

0.6875

0.7015

0.3886

0.5387

0.58

175

  

pp Ø

313 (63.9)

177 (36.1)

0.5743

0.942 (0.764–1.161)

101 (41.2)

111 (45.3)

33 (13.5)

0.7926

0.5014

0.9019

0.7477

0.77

245

  

pp male

133 (64.6)

73 (35.4)

0.5167

0.900 (0.655–1.237)

42 (40.8)

49 (47.6)

12 (11.7)

0.7250

0.8995

0.4775

0.4289

0.69

103

  

pp female

180 (63.4)

104 (36.6)

0.9694

0.995 (0.753–1.314)

59 (41.5)

62 (43.7)

21 (14.8)

0.6352

0.4961

0.3850

0.6777

0.48

142

 

control

Ø

1121 (65.3)

597 (34.7)

  

364 (42.4)

393 (45.8)

102 (11.9)

    

0.79

859

  

male

585 (66.9)

289 (33.1)

  

197 (45.1)

191 (43.7)

49 (11.2)

    

0.79

437

  

female

536 (63.5)

308 (36.5)

  

167 (39.6)

202 (47.9)

53 (12.6)

    

0.50

422

  1. Significance threshold: p = 0.025 (Bonferroni corrected for 2 SNPs). Significant values indicated by bold letter;
  2. 1CI = 95%. HWE: Hardy-Weinberg equilibrium, Pearson's goodness-of-fit chi-square (degree of freedom = 1).