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Table 4 Allele frequencies of single nucleotide polymorphism in IL-12B among male Graves disease patients with or without Graves ophthalmopathy

From: Association of IL12B polymorphisms with susceptibility to Graves ophthalmopathy in a Taiwan Chinese population

SNPs

GD/nonGO

GD/GO

P Valuea

Odds ratio (95% CI)b

Number (%)

Number (%)

rs2195940

    

 C/C

43 (89.58)

49 (96.08)

0.21

 

 C/T

5 (10.42)

2 (3.92)

  

 T/T

0 (0.00)

0 (0.00)

  

 C

91 (94.79)

100 (98.00)

0.22

 

 T

5 (5.21)

2 (2.00)

  

rs2853696

    

 A/A

0 (0.00)

0 (0.00)

--

 

 A/G

0 (0.00)

0 (0.00)

  

 G/G

48 (100.00)

51 (100.00)

  

 A

0 (0.00)

0 (0.00)

--

 

 G

96 (100.00)

102 (100.00)

  

rs2421047

    

 A/A

9 (18.75)

6 (11.76)

0.18

 

 A/G

32 (66.67)

30 (58.82)

  

 G/G

7 (14.58)

15 (29.41)

  

 A

50 (52.08)

42 (41.18)

0.12

 

 G

46 (47.92)

60 (58.82)

  

rs2853694

    

 A/A

26 (54.17)

21 (41.18)

0.25

 

 A/C

20 (41.67)

24 (47.06)

  

 C/C

2 (4.16)

6 (11.76)

  

 A

72 (75.00)

66 (64.71)

0.11

 

 C

24 (25.00)

36 (35.39)

  

rs2569254

    

 C/C

32 (66.67)

33 (64.71)

0.38

 

 C/T

16 (33.33)

16 (31.37)

  

 T/T

0 (0.0)

2 (3.92)

  

 C

80 (83.33)

82 (80.39)

0.59

 

 T

16 (16.67)

20 (19.61)

  

rs1003199

    

 C/C

23 (47.92)

13 (25.49)

0.01

1

 C/T

23 (47.92)

28 (54.90)

 

4.11 (0.82-20.66)

 T/T

2 (4.16)

10 (19.61)

 

8.85 (1.68-46.69)

 C

69 (71.88)

54 (52.94)

6.00×10-3

1

 T

27 (28.12)

48 (47.06)

 

2.27 (1.26-4.10)

rs7709212

    

 C/C

14 (29.17)

12 (23.53)

0.82

 

 C/T

27 (56.25)

31 (60.78)

  

 T/T

7 (14.58)

8 (15.69)

  

 C

55 (57.29)

55 (53.92)

0.63

 

 T

41 (42.71)

47 (46.08)

  

rs6868898

    

 C/C

5 (10.42)

10 (19.61)

0.19

 

 C/T

18 (37.50)

23 (45.10)

  

 T/T

25 (52.08)

18 (35.29)

  

 C

28 (29.17)

43 (42.16)

0.06

 

 T

68 (70.83)

59 (57.84)

  
  1. Abbreviations: SNP, single nucleotide polymorphism; GD, Graves disease; GO, Graves ophthalmopathy; CI, confidence interval.
  2. aP values (two-tailed) were calculated using chi-square tests with 3× 2 contingency tables (genotypes; 2 d.f.) or 2× 2 contingency tables (alleles; 1 d.f.).
  3. bOdds ratios and 95% CI per genotype and allele were estimated by applying unconditional logistic regression. P values less than 0.05 were considered significant.