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. 2020 Jul 31;3:410. doi: 10.1038/s42003-020-01137-3

Table 3.

Testing seven CCT-associated loci for keratoconus-susceptibility.

Gene Chr Position SNP Effect allele Control Keratoconus Odds ratio (95% CI) Pa
N EAF N EAF
NRXN1 2 50635086 rs13382330 C 8137 0.176 179 0.159 0.89 (0.67–1.19) 0.420
CPLX2 5 175244097 rs4242187 T 8150 0.097 179 0.070 0.70 (0.46–1.05) 0.082
CSMD1 8 2799288 rs143428993 A 8148 0.012 179 0.017 1.39 (0.61–3.14) 0.435
ADAM12 10 127905962 rs11244890 A 8156 0.211 179 0.196 0.91 (0.70–1.19) 0.491
SMAD3 15 67467507 rs12913547 T 8096 0.563 179 0.651 1.44 (1.16–1.80) 0.001b
WWOX 16 78430702 rs6564538 T 8156 0.110 179 0.117 1.07 (0.77–1.48) 0.680
CDH13 16 83650510 rs1035533 G 8150 0.190 179 0.201 1.07 (0.83–1.39) 0.594

Chr, chromosome; EAF, effect allele frequency; SNP, single-nucleotide polymorphism; CI, confidence interval.

aP-values derived using logistic-regression analysis.

bP-values are statistically significant after Bonferroni’s correction.