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

BMC Med Genet · 2008 · PMC2438340 · PMID 18547406

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closest p

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The sentences

borderline significantno p-value reported

The frequency of one variant; hMSH2 c.-118 T>C differed significantly between the sporadic CRC cases and the sub-cohort with a borderline significant p -value of 0.0037 (significance level: 0.05/13 = 0.0038).

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