Table 3.
Gene | SNP | Minor allele | Alternative allele | UNAFF Counta | AFF Countb | OR (95% CI) c | Pca_BHd | Pm_BHe |
---|---|---|---|---|---|---|---|---|
IL-10 | rs1518111 | G | A | 52/193/150 | 15/89/58 | 1.18 (0.78, 1.79) | 0.78 | 0.65 |
IL-10 | rs3021094 | G | T | 72/208/103 | 24/90/41 | 0.77 (0.49, 1.19) | 0.73 | 0.48 |
IL-10 | rs1800893 | T | C | 5/125/260 | 3/90/68 | 2.84 (1.66, 4.95) | 3.00E-06 | 0.002 |
CYP1B1 | rs1056836 | G | C | 8/109/267 | 1/41/113 | 0.74 (0.39, 1.34) | 0.62 | 0.55 |
IL-1RN | rs4251961 | C | T | 4/73/311 | 7/46/109 | 2.54 (1.43, 4.58) | 0.002 | 0.007 |
OGG1 | rs1052133 | G | C | 89/186/123 | 31/99/32 | 1.11 (0.74, 1.69) | 0.49 | 0.79 |
OGG1 | rs293795 | G | A | 1/30/386 | 2/22/145 | 1.73 (0.85, 3.53) | 0.03 | 0.31 |
IL-4 | rs2243267 | C | G | 14/180/188 | 6/75/74 | 1.01 (0.61, 1.66) | 0.78 | 0.98 |
TNF | rs1041981 | T | G | 72/207/105 | 32/93/30 | 1.34 (0.88, 2.05) | 0.32 | 0.39 |
TNF | rs1800630 | T | G | 16/101/270 | 2/77/83 | 2.35 (1.4, 3.98) | 0.01 | 0.007 |
TNF | rs1800629 | A | G | 2/61/319 | 1/20/134 | 0.37 (0.17, 0.76) | 0.73 | 0.03 |
PON1 | rs3917567 | C | T | 4/74/317 | 4/29/129 | 1.06 (0.57, 1.96) | 0.73 | 0.89 |
PON1 | rs662 | A | G | 51/191/142 | 20/74/61 | 0.68 (0.44, 1.03) | 0.73 | 0.20 |
PON1 | rs13306698 | C | T | 0/18/379 | 0/46/116 | 10.82 (4.34, 28.88) | 2.01E-14 | 2.00E-05 |
PON1 | rs854560 | T | A | 2/26/356 | 0/15/140 | 0.84 (0.3, 2.23) | 0.73 | 0.89 |
NAT2 | rs1799931 | A | G | 6/90/288 | 1/22/139 | 0.27 (0.13, 0.54) | 0.02 | 0.003 |
CYP2E1 | rs743534 | C | A | 12/109/262 | 2/37/116 | 0.82 (0.45, 1.48) | 0.30 | 0.72 |
CYP2E1 | rs2480258 | C | T | 104/166/129 | 44/57/64 | 0.97 (0.69, 1.36) | 0.73 | 0.89 |
RAG1 | rs3740955 | A | G | 16/141/255 | 8/67/92 | 1.55 (0.97, 2.48) | 0.35 | 0.20 |
ERCC5 | rs17655 | C | G | 89/191/104 | 40/74/41 | 1.22 (0.82, 1.82) | 0.73 | 0.55 |
NQO1 | rs1800566 | T | C | 80/197/107 | 39/72/44 | 1.21 (0.81, 1.8) | 0.73 | 0.55 |
BRCA1 | rs1799966 | G | A | 45/194/156 | 14/95/53 | 0.95 (0.6, 1.49) | 0.73 | 0.89 |
UNAFF is the count of genotypes (rare homozygosity/ heterozygosity /common homozygosity) in controls;
AFF is the count of genotypes in cases.
OR, odds ratio; 95% CI, 95% confidence interval.
Pca_BH is the p-value of Cochran-Armitage trend test adjusted by BH method.
Pm_BH is the p-value adjusted by BH method using multivariable logistic model adjusted for age, gender, education, family history of cancer and BMI. Bolded variables are statistically significant adjusted by BH method in either univariate or multiple logistic analysis.