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Table 4 The p-values of marginal Fisher's exact tests between groups

From: The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population

Id Variant Sporadic-Sub-cohort Familiar-Sub-cohort Sporadic-familiar All
  MLH1     
23 c.307-29 C>A 0.7259 1.0000 0.6673 0.8632
25 c.453+79 A>G 0.7908 - - -
24 c.350 C>T - 0.2988 - -
26 c.545+43 C>G 0.3263 1.000 1.000 0.4741
27 c.655 A>G 0.7715 0.5619 0.4869 0.7489
28 c.790+10 A>G 1.0000 - - -
29 C884+39G>A - 0.2943 - -
85 c.1217 G>A 1.0000 0.5359 0.4858 0.4833
31 c.1379 A>C - 0.1880 - -
32 c.1558+14 G>A 1.0000 0.6063 0.7685 0.8722
37 c.1668-19 A>G 0.5382 0.0044 0.0329 0.0148
33 c.1732-2 A>T - 0.3109 - -
34 c.1852_1853 AA>GC 0.2408 0.5672 0.6760 0.3569
100 c.1942 C>T - 0.4747   
35 c.1959 G>T 0.2473 1.0000 0.3642 0.4493
36 c.2152 C>T - 0.0840 - -
  MSH2     
89 c.-118 T>C 0.0037 - - -
41 c.965 G>A 0.2574 0.0244 0.3609 0.0582
43 c.1511-9 A>T 0.0958 0.7314 0.0796 0.1617
  1. The Bonferroni corrected p-value of sporadic versus sub-cohort is 0.05/13 = 0.0038
  2. The Bonferroni corrected p-value of familiar-versus sub-cohort is 0.05/15 = 0.0033
  3. Polymorphic variants with borderline significant p-values are in bold