Official Journal of the Human Genome Organisation
Table 2 Analysis of the association of SNP with cancer susceptibility under a recessive model of inheritance in the combined Swedish and Finnish samples
Sample | Size | Genotype Freq (%) | OR (95% CI) | P value | |
|---|---|---|---|---|---|
GG or GT | TT | ||||
Controls | 2,739 | 97.08 | 2.92 | ||
All cases | 3,512 | 96.07 | 3.93 | 1.34 (1.01, 1.77) | 0.04 |
ER+ cases | 2,492 | 96.27 | 3.73 | 1.26 (0.92, 1.72) | 0.15 |
ER− cases | 588 | 95.58 | 4.42 | 1.48 (0.93, 2.35) | 0.10 |
Postmenopausal cases | 2,447 | 96.24 | 3.76 | 1.30 (0.96, 1.76) | 0.10 |
Premenopausal cases | 502 | 94.82 | 5.18 | 1.66 (1.00, 2.75) | 0.05 |
Sporadic cases | 2,359 | 96.31 | 3.69 | 1.25 (0.92, 1.70) | 0.16 |
Familial cases | 1,098 | 95.72 | 4.28 | 1.48 (1.01, 2.17) | 0.04 |