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. Author manuscript; available in PMC: 2010 Sep 27.
Published in final edited form as: Cancer Genet Cytogenet. 2008 Jun;183(2):94–98. doi: 10.1016/j.cancergencyto.2008.02.008

Table 2.

Combined effects of risk variants

Model Case/control OR (95% CI)a p-valuea
Number of risk allele
 0–3 151/115 Reference -
 4 183/127 1.16 (0.83 – 1.63) 0.3762
 5 290/156 1.47 (1.08 – 2.02) 0.0160
 6 305/155 1.58 (1.15– 2.17) 0.0044
 7 244/121 1.60 (1.15 – 2.22) 0.0057
 8 168/74 1.82 (1.26 – 2.64) 0.0015
 9–11 118/46 1.99 (1.30 – 3.04) 0.0014
 Per allele 1.11 (1.05 – 1.16) < 0.0001
 P-value for trend < 0.0001

Percentage of carrying risk allele
 Q1 (≤ 0.417) 464/319 Reference -
 Q2 (> 0.417 and ≤ 0.5) 346/176 1.35 (1.07 – 1.71) 0.0114
 Q3 (> 0.5 and ≤ 0.6) 259/133 1.36 (1.05 – 1.76) 0.0190
 Q4 (> 0.6 ) 390/166 1.61 (1.28 – 2.04) < 0.0001
 P-value for trend < 0.0001
a

Adjusted for age and geographical region using the logistic regression