Research Article
Association of HER1 and HER2 Gene Variants in the Predisposition of Colorectal Cancer
Table 3
HER1 and HER2 SNPs' genotype and allele frequencies in colorectal cancer cases and the control population based on age.
| SNP ID | Genotype | Controls n (frequency) | Colorectal cancer n (frequency) | OR (95% CI) | χ2 value | p∗ value |
| ≤58 | | | | | | | rs763317 HER1 | AA | 22 (0.29) | 16 (0.23) | Ref | | | GA | 46 (0.6) | 41 (0.58) | 1.226 (0.568-2.645) | 0.27 | 0.60413 | GG | 9 (0.12) | 14 (0.2) | 2.139 (0.744-6.151) | 2.02 | 0.15540 | Allele | | | | | | A | 90 (0.58) | 73 (0.51) | Ref | | | G | 64 (0.42) | 69 (0.49) | 1.329 (0.840-2.104) | 1.48 | 0.22426 |
| rs3752651 HER1 | TT | 60 (0.71) | 53 (0.74) | Ref | | | CT | 20 (0.24) | 19 (0.26) | 1.075 (0.519-2.228) | 0.04 | 0.84480 | CC | 4 (0.05) | 0 (0) | 0.126 (0.007-2.388) | 3.43 | 0.06403 | Allele | | | | | | T | 140 (0.83) | 125 (0.87) | Ref | | | C | 28 (0.17) | 19 (0.13) | 0.760 (0.405-1.428) | 0.73 | 0.39268 |
| rs1058808 HER2 | GG | 30 (0.36) | 22 (0.31) | Ref | | | CG | 44 (0.53) | 32 (0.46) | 0.992 (0.486-2.026) | 0.00 | 0.98183 | CC | 9 (0.11) | 16 (0.23) | 2.424 (0.906-6.490) | 3.18 | 0.07462 | Allele | | | | | | G | 104 (0.63) | 76 (0.54) | Ref | | | C | 62 (0.37) | 64 (0.46) | 1.413 (0.894-2.232) | 2.19 | 0.13855 |
| rs1136201 HER2 | AA | 65 (0.78) | 62 (0.87) | Ref | | | AG | 17 (0.2) | 9 (0.13) | 0.555 (0.230-1.338) | 1.75 | 0.18580 | GG | 1 (0.01) | 0 (0) | 0.349 (0.014-8.737) | 0.95 | 0.33054 | Allele | | | | | | A | 147 (0.89) | 133 (0.94) | Ref | | | G | 19 (0.11) | 9 (0.06) | 0.524 (0.229-1.197) | 2.42 | 0.12010 |
| >58 | | | | | | | rs763317 HER1 | AA | 21 (0.29) | 24 (0.35) | Ref | | | GA | 36 (0.5) | 32 (0.46) | 0.778 (0.366-1.654) | 0.43 | 0.51372 | GG | 15 (0.21) | 13 (0.19) | 0.758 (0.295-1.953) | 0.33 | 0.56612 | Allele | | | | | | A | 78 (0.54) | 80 (0.58) | Ref | | | G | 66 (0.46) | 58 (0.42) | 0.857 (0.535-1.372) | 0.41 | 0.51996 |
| rs3752651 HER1 | TT | 59 (0.75) | 49 (0.69) | Ref | | | CT | 18 (0.23) | 22 (0.31) | 1.472 (0.710-3.051) | 1.08 | 0.29770 | CC | 2 (0.03) | 0 (0) | 0.240 (0.011-5.126) | 1.64 | 0.20083 | Allele | | | | | | T | 136 (0.86) | 120 (0.85) | Ref | | | C | 22 (0.14) | 22 (0.15) | 1.133 (0.598–2.149) | 0.15 | 0.70134 |
| rs1058808 HER2 | GG | 32 (0.42) | 22 (0.32) | Ref | | | CG | 37 (0.48) | 39 (0.57) | 1.533 (0.758–3.103) | 1.42 | 0.23381 | CC | 8 (0.1) | 8 (0.12) | 1.455 (0.474–4.459) | 0.43 | 0.51096 | Allele | | | | | | G | 101 (0.66) | 83 (0.6) | Ref | | | C | 53 (0.34) | 55 (0.4) | 1.263 (0.784–2.033) | 0.92 | 0.33644 |
| rs1136201 HER2 | AA | 58 (0.73) | 58 (0.83) | Ref | | | AG | 20 (0.25) | 12 (0.17) | 0.600 (0.269–1.339) | 1.57 | 0.20989 | GG | 1 (0.01) | 0 (0) | 0.333 (0.013–8.352) | 0.99 | 0.31937 | Allele | | | | | | A | 136 (0.88) | 128 (0.91) | Ref | | | G | 22 (0.14) | 12 (0.09) | 0.580 (0.276–1.219) | 2.10 | 0.14691 |
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OR 95% CI, odds ratio and 95% confidence interval. was considered significant and are depicted in bold. |