SNP rs no. | Allele | Minor Allele Frequency | |||
---|---|---|---|---|---|
1 | 2 | Cases, n = 451 | Controls, n = 392 | OR (95% CI) | |
1004819 | T | C | 0.414 | 0.419 | 1.03 (0.81–1.31) |
7517487 | T | G | 0.391 | 0.414 | 1.11 (0.88–1.41) |
10489629 | A | G | 0.263 | 0.255 | 1.03 (0.80–1.33) |
2201841 | C | T | 0.267 | 0.257 | 1.04 (0.81–1.34) |
11456804 | T | G | — | — | 0.91 (0.57–1.45) |
11209026 | G | A | — | — | 1.03 (0.80–1.33) |
1343151 | C | T | 0.043 | 0.048 | 0.97 (0.76–1.22) |
10889677 | A | C | 0.268 | 0.260 | 1.01 (0.80–1.28) |
11209032 | G | A | 0.497 | 0.489 | 1.03 (0.81–1.31) |
1495965 | G | A | 0.492 | 0.494 | 1.11 (0.88–1.41) |
↵* Study population was 854 subjects (451 cases and 391 controls) and 8 SNP with 13 missing values. Two SNP (rs11456804, rs11209026) were not polymorphic. SNP: single-nucleotide polymorphism.