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Table 4 Distribution of genotypic, allelic frequencies and genetic models of LHCGR variants (rs2293275 and rs12470652) between PCOS cases and controls

From: Association analysis of LHCGR variants and polycystic ovary syndrome in Punjab: a case–control approach

SNP

Genotype/ Allele

Case (%)

Control (%)

χ2 p-value

OR

(95% CI)

p-value

rs2293275

GG

138 (32.8)

120 (37.2)

 

Reference

 
 

GA

162 (38.4)

135 (42)

0.04*

1.04

0.7 to 1.45

0.8

 

AA

121 (28.8)

67 (20.8)

 

1.7

(1.15 to 2.5)

0.006*

 

G

438 (52)

374 (58)

0.02*

Reference

 
 

A

404 (48)

270 (42)

 

1.3 (1.03 to 1.5)

0.02*

Dominant model

G/G

G/A + A/A

138

283

120

203

0.2

-

0.21

0.89 to 1.64

-

0.2

Recessive model

G/A + G/G

A/A

300

121

255

67

0.01*

-

1.53

1.09 to 2.16

-

0.01*

Heterozygous model

G/G + A/A

G/A

259

162

186

136

0.34

-

0.85

0.63 to 1.14

-

0.3

rs12470652

TT

402 (95)

314 (97.5)

 

Reference

 
 

TC

11 (3)

7 (2.2)

0.13

1.2

(0.47 to 3.2)

0.67

 

CC

8 (2)

1 (0.3)

 

6.2

(0.7 to 50.2)

0.08

 

T

815 (97)

635 (98.6)

0.02*

Reference

 
 

C

27 (3)

9 (1.4)

 

2.3

(1.09to 5.3)

0.02*

Dominant model

T/T

T/C + C/C

402

19

314

8

0.14

-

1.8

(0.8 to 4.2)

-

0.14

Recessive model

T/T + T/C

C/C

413

8

321

1

0.04*

-

6.2

(0.77 to 49.7)

-

0.08

Heterozygous model

T/T + C/C

T/C

410

11

315

7

0.69

-

1.2

(0.4 to 3.1)

-

0.7

  1. χ2 – chi square, OR Odds ratio, *p < 0.05 Significant