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Table 3 Association between CCT-associated SNPs and KC risk in the Saudi Arabian study population

From: Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population

Locus

Lead SNP

A1/A2

MA

MAF Case

MAF Control

p-value

OR (95 % CI)

COL4A3

rs7606754

A/G

A

0.35

0.37

0.6

0.9 (0.7-1.3)

FNDC3B

rs4894535

C/T

T

0.16

0.12

0.1

1.4 (0.9-2,2)

MPDZ-NF1B

rs1324183

A/C

A

0.25

0.28

0.4

0.8 (0.8-1.2)

RXRA-COL5A1

rs1536482

A/G

A

0.45

0.41

0.4

1.1 (0.8-1.6)

COL5A1

rs7044529

C/T

T

0.14

0.13

0.8

1.1 (0.7-1.7)

LCN12-PTGDS

rs11145951

C/T

T

0.44

0.49

0.2

0.8 (0.6-1.1)

FOXO1

rs2721051

C/T

T

0.14

0.11

0.2

1.4 (0.9-2.2)

BANP-ZNF49

rs9938149

A/C

C

0.29

0.32

0.4

0.9 (0.6-1.2)

  1. CCT Central cornea thickness; SNP single nucleotide polymorphism; KC keratoconus; A1/A2 Allele 1/Allele 2; MA minor allele; MAF minor allele frequency; p-value, derived from two-tailed fisher exact test; OR odds ratio; CI confidence interval. COL4A3 Collagen, type IV, alpha (Goodpasture antigen); FNDC3B fibronectin type III domain containing 3B; MPDZ multiple PDZ domain protein; NF1B neurofibromin 1b; COL5A1 collagen, type V, alpha 1; LCN12 lipocalin 12; PTGDS prostaglandin D2 synthase 21 kDa; FOXO1 forkhead box O1; BANP BTG3 associated nuclear protein; ZNF469 zinc finger protein 469