Table 1 Association analysis results for the top 15 SNPs in the discovery cohort.

From: Identification of regulatory variants associated with genetic susceptibility to meningococcal disease

SNP

Chr

Location

Risk allele

Freq in cases

Freq in control

P-value

Odds ratio

OR – 95% CI

OR + 95% CI

rs12476782

2

191472880

A

0.26

0.16

2.38 × 10−4

1.9

1.4

2.6

rs11625840

14

22627848

A

0.38

0.26

2.66 × 10−4

1.7

1.3

2.3

rs2242543

14

22694331

A

0.36

0.25

3.77 × 10−4

1.7

1.3

2.4

rs79840975

18

56209387

T

0.02

0.08

4.06 × 10−4

0.3

0.1

0.5

rs11585994

1

8258226

C

0.16

0.26

4.18 × 10−4

0.5

0.4

0.8

rs988997

14

22693832

G

0.36

0.25

4.57 × 10−4

1.7

1.3

2.3

rs10488042

7

101652458

A

0.19

0.11

4.87 × 10−4

2.1

1.4

3.1

rs7130129

11

65354926

A

0.42

0.54

5.27 × 10−4

0.6

0.5

0.8

rs2240985

2

37899654

A

0.08

0.16

8.07 × 10−4

0.5

0.3

0.7

rs11228991

11

57078876

G

0.12

0.06

8.76 × 10−4

2.4

1.4

3.9

rs12717364

14

22693912

C

0.50

0.38

9.86 × 10−4

1.6

1.2

2.0

rs13379037

14

22693679

C

0.50

0.38

1.03 × 10−3

1.6

1.2

2.0

rs2595370

18

29239527

A

0.09

0.16

1.09 × 10−3

0.5

0.3

0.7

rs2468842

11

18154120

A

0.16

0.26

1.12 × 10−3

0.6

0.4

0.8

rs4823231

22

46088119

T

0.16

0.25

1.12 × 10−3

0.6

0.4

0.8

  1. Chr: chromosome, Freq: Frequency, OR: Odds Ratio, CI: Confidence Interval.