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Table 3 Association between MHC single nucleotide polymorphisms (SNP) and Behçet’s disease in the full dataset and on the subset allelotyped for HLA-B

From: Characterization of the major histocompatibility complex locus association with Behçet’s disease in Iran

Dataset

dbSNP ID

Gene or

Allele

Frequency

P unadj -values

P adj -values

Odds ratio (95% CI)

  

nearest gene

 

Cases

Controls

   

Total

rs9260997

HLA-G/H/J

C

0.911

0.886

2.03 × 10 −2

2.20 × 10 −2

1.31 (1.04, 1.67)

 

rs76546355

HLA, B - MICA

A

0.388

0.140

2.51 × 10 −69

9.34 × 10 −68

4.56 (3.78, 5.50)

 

rs2848713

MICA

A

0.422

0.184

2.12 × 10 −56

4.90 × 10 −55

3.52 (2.97, 4.18)

HLA-B allelotyped

rs9260997

HLA-G/H/J

C

0.908

0.886

1.06 × 10−1

1.00 × 10−1

 
 

rs76546355

HLA-B - MICA

A

0.388

0.126

9.84 × 10 −47

1.78 × 10 −46

5.46 (4.21, 7.09)

 

rs2848713

MICA

A

0.427

0.184

4.83 × 10 −35

7.14 × 10 −35

3.73 (2.97, 4.69)

  

HLA-B

B*51

0.391

0.121

5.86 × 10 −48

8.34 × 10 −48

5.44 (4.20, 7.05)

  1. For comparison, the association of the human leukocyte antigen (HLA)-B*51 allele using a log-additive model of association, unadjusted (P unadj) and adjusted (P adj) for gender, is shown at the bottom of the table. Nominally significant P-values are highlighted in bold and the respective odds ratios and 95% CI are indicated for the adjusted model.