Skip to main content

Table 2 Association of PRKCD rs74437127 and CARD9 rs3812555 with VKH diseases

From: Genetic association of PRKCD and CARD9 polymorphisms with Vogt–Koyanagi–Harada disease in the Chinese Han population

Gene

SNPs

Genotype allele

VKH n (%)

Control n (%)

P value

Pc value

OR(95% CI)

PRKCD

rs74437127

TT

0 (0.000)

7 (0.008)

0.007*

NS

  

TC

73 (0.080)

97 (0.111)

0.026

NS

0.698 (0.507–0.960)

  

CC

839 (0.920)

771 (0.881)

0.006

NS

1.550 (1.132–2.124)

  

T

73 (0.040)

111 (0.063)

0.001

0.020

0.616 (0.455–0.833)

  

C

1751 (0.960)

1639 (0.937)

0.001

0.020

1.624 (1.200–2.199)

CARD9

rs3812555

CC

695 (0.840)

602 (0.744)

1.57 × 10–6

2.04 × 10–5

1.810 (1.418–2.311)

  

TC

119 (0.144)

187 (0.231)

6.04 × 10–6

7.85 × 10–5

0.559 (0.434–0.721)

  

TT

13 (0.016)

20 (0.025)

0.221*

NS

0.630 (0.311–1.275)

  

C

1509 (0.912)

1391 (0.860)

2.12 × 10–6

2.76 × 10–5

1.698 (1.362–2.118)

  

T

145 (0.088)

227 (0.140)

2.12 × 10–6

2.76 × 10–5

0.589 (0.472–0.734)

  1. VKH, VKH disease; OR, odds ratio; 95% CI, 95% confidence interval; NS, not significant; Pc value, P value with Bonferroni correction; Pc value < 0.05 was regarded to have statistical significance; * Fischer's exact test