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. 2019 Jan 27;2019:2604386. doi: 10.1155/2019/2604386

Table 3.

Single-nucleotide polymorphism allele frequencies and associations for 12 SNPs between cases and controls.

SNP CHR BP MA MAF case MAF control P values OR (95% CI)
rs1676486 1 103354138 A 0.32 0.19 0.026 2.089 (1.092–3.996)
rs3753841 1 103379918 G 0.39 0.26 0.036 1.886 (1.038–3.426)
rs12138977 1 103393457 C 0.31 0.18 0.024 2.133 (1.104–4.123)
rs2126642 1 103405793 A 0.11 0.10 0.818 1.112 (0.450–2.746)
rs2622848 1 103421003 C 0.10 0.07 0.449 1.475 (0.539–4.040)
rs216489 11 16823736 G 0.41 0.38 0.668 1.131 (0.645–1.982)
rs1027617 11 16842787 A 0.38 0.45 0.321 0.754 (0.431–1.317)
rs366590 11 16872440 A 0.23 0.20 0.607 1.194 (0.608–2.343)
rs11024060 11 16881961 T 0.29 0.36 0.297 0.732 (0.407–1.316)
rs6486330 11 16990290 T 0.20 0.19 0.859 1.065 (0.530–2.142)
rs11024097 11 16999029 C 0.36 0.45 0.200 0.693 (0.395–1.215)
rs11024102 11 17008605 C 0.44 0.41 0.671 1.128 (0.647–1.965)

Chi-square tests and logistic regression were used. CHR: chromosome; BP: base pair position; MA: minor allele; MAF: minor allele frequency; MAF Case: minor allele frequencies in cases; MAF Control: minor allele frequencies in controls; OR: odds ratio; CI: confidence interval.