Table 2.
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.