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. 2019 Dec 5;40(9):1734–1741. doi: 10.1097/IAE.0000000000002682

Table 2.

Analysis of Eight SNPs in Severe cCSC

SNP (Locus) Alleles in Controls (Major/Minor) Severe cCSC (n) MAF in Severe cCSC Controls (n) MAF Among Controls Unadjusted Allelic P Allelic OR (95% CI)
rs10490924 (ARMS2) G/T 171 0.187 812 0.217 0.214 0.83 (0.62–1.11)
rs2070951 (NR3C2) C/G 172 0.494 1,385 0.468 0.350 1.11 (0.89–1.39)
rs800292 (CFH) G/A 172 0.372 798 0.235 0.0014* 1.93 (1.51–2.47)
rs1061170 (CFH) T/C 172 0.282 803 0.353 0.012 0.72 (0.56–0.93)
rs1065489 (CFH) G/T 172 0.096 794 0.177 2.22 × 10−4* 0.49 (0.34–0.72)
rs1329428 (CFH) C/T 171 0.588 787 0.429 0.0010* 1.89 (1.49–2.40)
rs2284664 (CFH) C/T 171 0.316 805 0.219 1.21 × 10−4* 1.65 (1.28–2.13)
rs3753394 (CFH) C/T 171 0.202 800 0.293 6.10 × 10−4* 0.61 (0.46–0.81)
*

Two-sided P values < 0.00556 were considered significant after correction for multiple testing.

ARMS2, age-related maculopathy susceptibility 2; CFH, complement factor H; MAF, minor allele frequency; NR3C2, nuclear receptor subfamily 3 Group C member 2.