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. 2019 Dec 12;2019:5284867. doi: 10.1155/2019/5284867

Table 4.

Genotypic association analysis in 135 residents with unexplained mild visual impairment (UMVI) and 133 residents with normal vision (NV).

SNP Genotype UMVI residents NV residents HWpval p value OR (95% CI) p value# OR# (95% CI)
number number
rs10865710 GG 36 0 0.08 7.17E − 42 NA
GC 91 14 6.40 (3.47–11.80) 1.86E − 41 0.01 (0.00–0.02)
CC 8 119 0.07 (0.03–0.14) (CC: GG + GC)
rs1801282 GG 0 0 1 NA NA
GC 22 0 NA 7.46E − 6 0.46 (0.40, 0.53)
CC 113 133 0.86 (0.61–1.21) (CC: GG + GC)
rs709158 GG 25 4 0.33 3.35E − 09 4.43 (1.46–13.43) 0.41 2.22 (0.67, 7.38)
GA 45 16 1.94 (1.00–3.78) 6.9E − 7 20.46 (5.84, 71.61)
AA 11 36 0.21 (0.10–0.45) 1.39E − 6 0.11 (0.04, 0.26)
rs3856806 TT 16 0 0.10 1.24E − 10 NA
TC 56 21 2.63 (1.51–4.58) 8.92E − 10 0.16 (0.09–0.29)
CC 63 112 0.55 (0.37–0.82) (CC: TT + TC)

p value (chi-square test); OR (95% CI) (chi-square test); OR# (95 % CI); p value# (Bonferroni correction); OR' (Bonferroni correction); HWpval, Hardy–Weinberg equilibrium p value. OR = odds ratio; CI = confidence interval; NA, the odds ratio was not available where the number of individuals with two copies of the risk allele was zero. χ2 test.