Table 3.
SNP | |||||||||
---|---|---|---|---|---|---|---|---|---|
1111 | 1510 | 3572 | 6021 | 7592 | |||||
Haplotype Index | Haplo. Freq. | OR* (95% CI) | P† | Global P† | |||||
1 | 40.5 | G | C | T | C | A | 1.14 (1.02; 1.28) | 0.03 | 0.07 |
2 | 3.1 | C | G | G | C | C | 0.98 (0.72; 1.33) | 0.91 | |
3 | 23.2 | G | G | G | C | A | 0.93 (0.81; 1.07) | 0.32 | |
4 | 27.7 | G | G | G | C | C | 0.98 (0.86; 1.12) | 0.68 | |
OR ‡ (95% CI) | 0.89 (0.69; 1.15) | 1.13 (1.01; 1.27) | 1.10 (0.99; 1.23) | 0.84 (0.60; 1.18) | 0.97 (0.86; 1.10) | ||||
P¶ | 0.13 | 0.03 | 0.08 | 0.46 | 0.58 | ||||
Global P | 0.03 |
Odds ratio per copy of haplotype adjusted for age, sex, current smoking, education, diastolic blood pressure, body mass index, and hypertension.
Permutation-based P value from score test. P values for individual haplotypes test the null hypothesis that the odds of having WML of a particular haplotype are the same as that of all other haplotypes combined. The global P value tests the null hypothesis that the odds of having WML are the same for all haplotypes.
Odds ratio per copy of variant allele adjusted for age, sex, current smoking, education, diastolic blood pressure, body mass index, and hypertension.
adjusted for multiple tests.
Haplo. Freq.: Haplotype frequency. SNP: Single nucleotide polymorphism