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Table 3 Genotype frequencies of the Behçet's disease-associated single-nucleotide polymorphisms identified in this study

From: Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study

  

Number

  

SNP

Genotype

Cases

Controls

OR (95% CI)

P value

rs11206377

GG

62

36

2.29 (1.39–3.78)

0.0011 (GG versus AG+AA)

 

AG

66

77

  
 

AA

16

32

  

rs2061634

GG

32

8

4.79 (2.13–10.77)

0.000047 (GG versus CG+CC)

 

CG

66

66

  
 

CC

56

80

  

rs317711

CC

12

3

4.23 (1.17–15.32)

0.018 (CC versus GC+GG)

 

GC

53

34

  
 

GG

85

112

  

rs4936742

TT

47

23

2.60 (1.48–4.59)

0.00076 (TT versus CT+CC)

 

CT

67

79

  
 

CC

28

42

  

rs9513584

GG

32

14

2.69 (1.37–5.29)

0.0033 (GG versus AG+AA)

 

AG

66

70

  
 

AA

47

63

  
  1. Odds ratios (ORs) and P values were calculated for the frequency of the homozygous-risk genotype in patients compared with controls. CI, confidence interval; SNP, single-nucleotide polymorphism.