Table 1. Summary results for six SNPs selected for genotyping in stage 2.
RAFc |
P valueg |
||||||||
---|---|---|---|---|---|---|---|---|---|
Markera allele | Chrb position | Stage | Controls | Cases | Per allele ORd (95% CI) |
Het. ORe (95% CI) |
Hom. ORf (95% CI) |
Stage | Combined |
rs4657482 | 1 | UK1 | 0.32 | 0.39 | 1.39 (1.21–1.59) | 1.29 (1.07–1.57) | 2.03 (1.52–2.70) | 1.6 × 10−6 | |
G/A | 164098273 | UK2 | 0.33 | 0.36 | 1.14 (0.99–1.31) | 1.15 (0.94–1.41) | 1.29 (0.95–1.75) | 0.07 | 2.0 × 10−6 |
rs4699052 | 4 | UK1 | 0.60 | 0.67 | 1.38 (1.20–1.57) | 1.27 (0.95–1.70) | 1.82 (1.36–2.45) | 3.0 × 10−6 | |
T/C | 104357239 | UK2 | 0.61 | 0.66 | 1.21 (1.05–1.39) | 1.10 (0.81–1.48) | 1.40 (1.04–1.90) | 0.008 | 2.1 × 10−7 |
rs4624820 | 5 | UK1 | 0.55 | 0.64 | 1.47 (1.29–1.67) | 1.41 (1.08–1.84) | 2.12 (1.62–2.78) | 4.6 × 10−9 | |
G/A | 141661972 | UK2 | 0.54 | 0.62 | 1.37 (1.19–1.58) | 1.27 (0.96–1.67) | 1.83 (1.38–2.44) | 6.7 × 10−6 | 3.3 × 10−13 |
rs210138 | 6 | UK1 | 0.20 | 0.27 | 1.50 (1.30–1.74) | 1.40 (1.16–1.70) | 2.57 (1.77–3.73) | 4.5 × 10−8 | |
A/G | 33650516 | UK2 | 0.20 | 0.27 | 1.50 (1.28–1.75) | 1.58 (1.29–1.94) | 1.99 (1.31–3.01) | 6.6 × 10−7 | 1.1 × 10−13 |
rs995030 | 12 | UK1 | 0.80 | 0.90 | 2.29 (1.88–2.78) | 3.85 (1.37–10.82) | 8.41 (3.02–23.37) | 1.9 × 10−18 | |
A/G | 87414802 | UK2 | 0.80 | 0.91 | 2.55 (2.05–3.19) | 2.63 (0.94–7.31) | 6.70 (2.43–18.49) | 1.2 × 10−19 | 1.0 × 10−31 |
rs1508595 | 12 | UK1 | 0.83 | 0.92 | 2.55 (2.05–3.18) | 5.31 (1.26–22.31) | 12.9 (3.11–53.58) | 1.9 × 10−19 | |
A/G | 87510147 | UK2 | 0.83 | 0.93 | 2.69 (2.10–3.44) | 2.22 (0.67–7.31) | 6.05 (1.87–19.55) | 4.9 × 10−18 | 2.6 × 10−30 |
dbSNP rs number and nonrisk/risk associated alleles.
Chromosome and build 36 position.
Frequency of the risk allele.
OR, odds ratio.
OR in heterozygotes, relative to common homozygotes.
OR in homozygotes, relative to common homozygotes.
Cochran-Armitage test for trend.