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Table 3 The frequency of the alleles and genotypes for SNPs studied in cases and the controls

From: Investigating the importance of EGFR (− 216G/T), Exo1 (K589E) and LEP (− 2548G/A) gene polymorphisms with risk of lung cancer as potential diagnostic biomarker in Iranian population

Gene

SNP

Genotype

Cases, n (%)

Controls, n (%)

OR*

95% CI*

P*

EGFR

rs712829

GG

30 (30)

20 (20)

1.00 (Reference)

1.00

 

GT

55 (55)

25 (25)

0/682

0/299–1/555

0/362

TT

15 (15)

55 (55)

5/500

2/239–13/510

0/000

Alleles

     

G

115 (57/5)

62 (31)

1.00 (Reference)

1.00

 

T

85 (42/5)

138 (69)

2/976

1/557–5/691

0.001

Exo1

rs1047840

AA

20 (20)

5 (5)

1.00

1.00

 

GA

22 (22)

17 (17)

3/111

0/848–11/408

0/087

GG

58 (58)

78 (78)

5/391

1/690–17/200

0/004

Alleles

     

A

62 (31)

27 (13/5)

1.00 (Reference)

1.00

 

G

138 (69)

173 (86/5)

2/851

1/291–6/300

0.010

LEP

rs7799039

GG

16 (16)

13 (31)

1.00 (Reference)

1.00

 

GA

53 (53)

50 (53)

0/808

0/318–2/050

0/653

AA

31 (31)

37 (16)

0/641

0/240–1/709

0/374

Alleles

     

G

75 (37/5)

85 (42/5)

1.00 (Reference)

1.00

 

A

125 (62/5)

115 (57/5)

0/812

0/431–1/530

0.519

  1. P p-value < 0.05, CI Confidence Interval, OR Odds Ratio