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. 2016 Jun 8;6:136. doi: 10.3389/fonc.2016.00136

Table 2.

Minor allele frequencies (MAF) and age- and center-adjusted odds ratios for the associations between SNPs in insulin-like growth factor signaling genes and breast cancer risk.

Gene SNP Location Major allele Minor allele European (641 cases, 806 controls)
East Asian (305 cases, 168 controls)
MAF (controls) Odds ratio p-value q-valuea MAF (controls) Odds ratio p-value q-valuea
IGF1 rs6214 3′UTR G A 0.43 0.90 (0.77, 1.04) 0.16 0.47 0.49 0.83 (0.63, 1.09) 0.17 0.44
IGF1 rs1549593 Intron C A 0.16 0.76 (0.61, 0.95) 0.01 0.11 0.02 0.72 (0.25, 2.13) 0.56 0.68
IGF1 rs17727841 Intron C G 0.19 1.00 (0.82, 1.21) 0.96 0.99 0.19 0.73 (0.51, 1.03) 0.07 0.39
IGF1 rs2288378 Intron G A 0.25 1.06 (0.89, 1.26) 0.52 0.82 0.19 0.71 (0.50, 1.01) 0.06 0.39
IGF1 rs7136446 Intron A G 0.42 1.09 (0.93, 1.26) 0.29 0.61 0.19 0.71 (0.50, 1.01) 0.06 0.39
IGF1 rs2195239 Intron G C 0.25 0.98 (0.83, 1.17) 0.84 0.98 0.46 0.94 (0.72, 1.23) 0.65 0.75
IGF1 rs7956547 Intron A G 0.27 0.97 (0.82, 1.15) 0.71 0.89 0.18 0.71 (0.50, 1.02) 0.07 0.39
IGF1 rs1019731b Intron C A 0.15 0.67 (0.53, 0.84) <0.01 0.01 0.00 N/A N/A N/A
IGF1 rs12821878c Intron G A 0.24 0.73 (0.61, 0.88) <0.01 0.01 0.04 1.25 (0.63, 2.49) 0.53 0.68
IGFBP3 rs6670 3′UTR A T 0.23 0.95 (0.80, 1.14) 0.57 0.84 0.01 2.41 (0.82, 7.06) 0.11 0.40
IGFBP3 rs2453839 Intron A G 0.19 1.04 (0.87, 1.25) 0.66 0.89 0.24 0.83 (0.60, 1.14) 0.24 0.49
IGFBP3 rs3110697 Intron G A 0.43 0.93 (0.80, 1.08) 0.36 0.66 0.29 0.86 (0.64, 1.15) 0.30 0.55
IGFBP3 rs2471551 Intron G C 0.22 0.90 (0.75, 1.08) 0.26 0.61 0.02 1.77 (0.74, 4.24) 0.20 0.44
IGFBP3 rs2132572 Promoter region G A 0.21 1.00 (0.84, 1.20) 0.99 0.99 0.25 0.81 (0.59, 1.11) 0.18 0.44
IGF1R rs951715 Intron A G 0.34 1.14 (0.98, 1.33) 0.08 0.36 0.50 0.89 (0.68, 1.16) 0.38 0.59
IGF1R rs2229765 Exond G A 0.44 1.03 (0.89, 1.19) 0.73 0.89 0.33 0.99 (0.74, 1.32) 0.95 0.99
IGF1R rs8038415 Intron A G 0.49 1.00 (0.86, 1.15) 0.95 0.99 0.46 1.22 (0.93, 1.60) 0.15 0.44
IRS1 rs1801278 Exone G A 0.06 1.17 (0.87, 1.57) 0.31 0.61 0.02 0.39 (0.13, 1.16) 0.09 0.39
PI3KCB rs12493155 Intron G A 0.45 1.07 (0.92, 1.23) 0.40 0.67 0.48 0.88 (0.68, 1.15) 0.35 0.59
PI3KCB rs524164 Intron G A 0.47 0.90 (0.78, 1.04) 0.16 0.47 0.02 0.70 (0.26, 1.92) 0.49 0.68
PI3KCB rs10513055 Intron A C 0.23 0.85 (0.71, 1.01) 0.07 0.36 <0.01 0.58 (0.04, 9.37) 0.70 0.77
PI3KCB rs361072 Intron A G 0.47 0.90 (0.78, 1.05) 0.17 0.47 0.02 0.70 (0.26, 1.92) 0.49 0.68

SNPs with a q-value <0.05 are presented in bold.

aFalse discovery rate-adjusted p-value.

bGenotype frequencies of nCC = 509, nAC = 125, and nAA = 7 among European cases; nCC = 578, nAC = 210, and nAA = 18 among European controls.

cGenotype frequencies of nGG = 421, nAG = 195, and nAA = 25 among European cases; nGG = 461, nAG = 301, and nAA = 44 among European controls.

dSynonymous mutation.

eGly/Arg substitution.