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. 2020 Sep 1;5:34. doi: 10.1038/s41525-020-00141-0

Table 2.

Single nucleotide polymorphisms in AMD.

Genes SNP A1 A2 F_A1 F_U p-value OR 95% CI FDR BH
C2 rs1883025 C G 0.018 0.052 0.28 0.34 (0.067, 1.72) 0.31
C3 rs4420638 C G 0.25 0.16 0.10 1.74 (0.91, 3.35) 0.25
CETP rs10490924 A C 0.34 0.35 0.89 0.93 (0.54, 1.61) 0.85
CFB1 rs4151667 A T 0.027 0.052 0.50 0.51 (0.13, 2.11) 0.51
CFB2 rs641153 T C 0.12 0.094 0.67 1.28 (0.55, 2.99) 0.76
CFB3 rs12614 A G 0.027 0.13 0.0057 0.19 (0.053, 0.67) 0.015
CFH1 rs800292 A G 0.24 0.082 0.0012 3.45 (2.31, 5.63) 0.0048
CFH2 rs1410996 A G 0.39 0.16 0.00019 3.21 (2.16, 4.85) 0.00091
CFH3 rs1061170 T C 0.60 0.34 0.000064 3.03 (1.89, 4.57) 0.00085
CFI rs10033900 C T 0.55 0.45 0.18 1.48 (0.87, 2.50) 0.31
COL8A1 rs13095226 C T 0.13 0.11 0.83 1.16 (0.52, 2.58) 0.85
HTRA1 rs11200638 A G 0.51 0.26 0.00012 2.97 (1.70, 5.20) 0.00085
LIPC rs10468017 T C 0.28 0.29 0.88 0.95 (0.53, 1.68) 0.85
TIMP3 rs9621532 C A 0.0091 0.034 0.37 0.26 (0.028, 2.34) 0.31
TNFRSF10A rs13278062 C A 0.41 0.5 0.18 0.69 (0.41, 1.17) 0.31
VEGF A rs1413711 T C 0.47 0.46 0.89 1.07 (0.63, 1.80) 0.85

A1 minor allele, A2 major allele, F_A1 frequency of A1 in AMD, F_U frequency of A1 in controls, FDR BH false discovery rate correction using the Benjamini–Hochberg procedure, OR odds ratio for A1.