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Table 3 The association between TMOD1 and PTCSC2 polymorphisms and the risk of thyroid carcinoma

From: Suggestive evidence of the genetic association of TMOD1 and PTCSC2 polymorphisms with thyroid carcinoma in the Chinese Han population

SNP-ID

Model

Genotype

Case (%)

Control (%)

Adjusted by age and sex

OR (95% CI)

p

rs10982622

Codominant

AG

196 (38.4%)

231 (45.7%)

0.74 (0.57–0.96)

0.025

  

GG

245 (48.0%)

214 (42.3%))

1.00

 

rs925489

Allele

T

891 (87.4%)

918 (90.9%)

1

 
  

C

129 (12.6%)

92 (9.1%)

1.45 (1.09–1.92)

0.011

 

Codominant

CT

117 (22.9%)

88 (17.4%)

1.43 (1.05–1.95)

0.024

  

TT

387 (75.9%)

415 (82.2%)

1.00

 
 

Dominant

CC.CT

123 (24.1%)

90 (17.8%)

1.47 (1.08–1.99)

0.014

  

TT

387 (75.9%)

415 (82.2%)

1.00

 
 

Additive

/

/

/

1.47 (1.10–1.97)

0.009

rs965513

Allele

G

893 (87.7%)

918 (90.9%)

1.00

 
  

A

125 (12.3%)

92 (9.1%)

1.40 (1.05–1.86)

0.021

 

Codominant

AG

113 (22.2%)

88 (17.4%)

1.37 (1.00-1.87)

0.048

  

GG

390 (76.6%)

415 (82.2%)

1.00

 
 

Dominant

AA.AG

119 (23.4%)

90 (17.8%)

1.41 (1.04–1.92)

0.028

  

GG

390 (76.6%)

415 (82.2%)

1.00

 
 

Additive

/

/

/

1.42 (1.06–1.90)

0.019

  1. SNP: single nucleotide polymorphism; OR: odds ratio; 95% CI: 95% confidence interval
  2. p < 0.05 indicates statistical significance. /: indicates additive model