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. 2009 Oct 9;11(5):R152. doi: 10.1186/ar2828

Table 2.

Three-marker haplotype analysis of ITGAV single-nucleotide polymorphisms (rs10174098, rs3911238, rs3738919) in the Wellcome Trust Case Control Consortium, New Zealand and Oxford sample sets

rs10174098 rs3911238 rs3738919 Case, number (frequency) Control, number (frequency) P value OR (95% CI)
WTCCC
 1 1 2 866 (0.261) 1,451 (0.275) 0.19 0.94 (0.85-1.03)
 2 1 1 858 (0.259) 1,382 (0.262) 0.82 0.99 (0.90-1.09)
 1 2 1 792 (0.239) 1,226 (0.232) 0.43 1.04 (0.94-1.16)
 1 1 1 524 (0.158) 741 (0.140) 0.021 1.15 (1.02-1.30)
 2 1 2 219 (0.066) 405 (0.077) 0.070 0.85 (0.72-1.01)
New Zealand
 1 1 2 357 (0.244) 260 (0.263) 0.29 0.90 (0.75~1.09)
 2 1 1 364 (0.249) 240 (0.243) 0.73 1.03 (0.86~1.25)
 1 2 1 359 (0.246) 223 (0.225) 0.26 1.12 (0.92~1.35)
 1 1 1 241 (0.165) 170 (0.172) 0.60 0.95 (0.76~1.17)
 2 1 2 110 (0.075) 73 (0.074) 0.91 1.02 (0.75~1.39)
Oxford, UK
 1 1 2 310 (0.256) 252 (0.253) 0.80 1.03 (0.85-1.24)
 2 1 1 306 (0.253) 262 (0.262) 0.67 0.96 (0.79-1.16)
 1 2 1 335 (0.277) 251 (0.252) 0.16 1.15 (0.95-1.39)
 1 1 1 158 (0.130) 162 (0.162) 0.04 0.78 (0.62-0.99)
 2 1 2 78 (0.064) 57 (0.057) 0.47 1.14 (0.80-1.62)

Only haplotypes with frequency of at least 0.05 in controls are shown. CI, confidence interval; HWE, Hardy-Weinberg equilibrium; OR, odds ratio; WTCCC, Wellcome Trust Case Control Consortium.