Barely Significant
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Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study.

BMC Gastroenterol · 2010 · PMC2954942 · PMID 20920174

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borderline significantno p-value reported
Applying the Bonferroni correction for multiple testing the P trend of rs27647 in the joint population remained borderline significant (P trend = 0.0043 × 11 = 0.047), although neither the ORs for heterozygotes nor for the homozygotes remained statistically significant after correction.

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