Table 2. Allele frequencies of the CAV1–CAV2 variants among NTG patients and controls.
SNP | Alleles (1/2) |
Total |
Males |
Females |
|||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MAF |
P-value | OR (95%CI) |
MAF |
P-value | OR (95%CI) |
MAF |
P-value | OR (95%CI) | |||||
Cases (n=292) | Controls (n=352) | Cases (n=140) | Controls (n=193) | Cases (n=152) | Controls (n=159) | ||||||||
rs1052990 | T/G | 0.179 | 0.236 | 0.014 | 0.71 (0.54–0.93) | 0.192 | 0.223 | 0.331 | 0.83 (0.56–1.21) | 0.168 | 0.250 | 0.012 | 0.60 (0.41–0.90) |
rs4236601 | G/A | 0.000 | 0.000 | — | — | ||||||||
rs7795356 | C/T | 0.052 | 0.058 | 0.592 | 0.88 (0.54–1.42) | 0.040 | 0.052 | 0.461 | 0.75 (0.36–1.60) | 0.063 | 0.066 | 0.841 | 0.94 (0.49–1.78) |
1, major allele; 2, minor allele; CI, confidence interval; MAF, minor allele frequency; OR, odds ratio; SNP, single-nucleotide polymorphism.
P-values were calculated using a χ2-test 2 × 2 contingency table.