Barely Significant
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Pathway analysis comparison using Crohn's disease genome wide association studies.

BMC Med Genomics · 2010 · PMC2908056 · PMID 20584322

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highly significantno p-value reported
However, many questions remain on how to best approach this problem, such as whether there is a need to obtain a score to summarize association evidence at the gene level, and whether a pathway, dominated by just a few highly significant genes, is of interest.

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