Table 2.
Gene | SNP | Chr | Position | MA | MAF | HWE | OR (95%CI) | P_logit† | P_cox‡ |
---|---|---|---|---|---|---|---|---|---|
TGFBR3-CDC7 | rs1192415 | 1 | 91611540 | G | 0.165 | 0.165 | 1.37 (0.93–2.01) | 0.108 | 0.277 |
TMCO1 | rs4656461 | 1 | 165717968 | G | 0.018 | 0.130 | 2.25 (0.83–6.08) | 0.112 | 0.326 |
TMCO1 | rs7555523 | 1 | 165749742 | C | 0.018 | 0.130 | 2.24 (0.82–6.06) | 0.114 | 0.338 |
CDKN2B-AS1 | rs1063192 | 9 | 22003368 | G | 0.163 | 0.862 | 1.18 (0.80–1.74) | 0.399 | 0.216 |
CDKN2B-AS1 | rs523096 | 9 | 22019130 | G | 0.088 | 0.128 | 1.35 (0.83–2.21) | 0.223 | 0.190 |
CDKN2B-AS1 | rs7049105 | 9 | 22028802 | A | 0.319 | 0.511 | 1.18 (0.87–1.61) | 0.277 | 0.249 |
CDKN2B-AS1 | rs2157719 | 9 | 22033367 | G | 0.084 | 0.217 | 1.44 (0.87–2.36) | 0.156 | 0.172 |
CDKN2B-AS1 | rs4977756 | 9 | 22068653 | G | 0.194 | 1.000 | 1.33 (0.93–1.91) | 0.119 | 0.070 |
CDKN2B-AS1 | rs10116277 | 9 | 22081398 | G | 0.270 | 0.545 | 1.17 (0.85–1.62) | 0.344 | 0.774 |
ATOH7 | rs7916697 | 10 | 68232096 | A | 0.377 | 0.479 | 1.28 (0.96–1.71) | 0.099 | 0.126 |
ATOH7 | rs1900004 | 10 | 68241124 | A | 0.377 | 0.614 | 1.24 (0.93–1.67) | 0.147 | 0.190 |
ATOH7 | rs3858145 | 10 | 68252081 | G | 0.376 | 0.919 | 1.28 (0.95–1.72) | 0.107 | 0.067 |
SIX1/SIX6 | rs33912345 | 14 | 60509819 | A | 0.180 | 0.520 | 1.08 (0.75–1.56) | 0.673 | 0.579 |
SIX1/SIX6 | rs10483727 | 14 | 60606157 | C | 0.184 | 0.525 | 1.12 (0.78–1.61) | 0.533 | 0.567 |
Chr, chromosome; MA, minor allele; MAF, minor allele frequency; HWE, Hardy–Weinberg equilibrium; OR, odds ratio; CI, confidence interval. The position of each SNP was referred to NCBI build GRCh38.p7. †P_logit values were calculated by logistic regression adjusted with age, gender, baseline MD, follow-up IOP, CCT, AL from comparison of allele frequencies between progress group and non-progress group.‡P_cox values were calculated by cox regression adjusted with age, gender, baseline MD, follow-up IOP, CCT, AL from comparison of patients with 1 or 2 risk alleles versus with 0 risk allele.