IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease.

Gastroenterology · 2007 · PMC2696256 · PMID 17484863

Europe PMC DOI

hedged sentence

0.0000

closest p · 0.0× alpha

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boldest claim

The sentences

highly significantP = 1.1 × 10 −12actually significant

Results: A highly significant association with CD was observed, with the strongest signal at coding variant Arg381Gln (allele frequency, 2.5% in CD vs 6.2% in controls [ P = 1.1 × 10 −12 ]; odds ratio, 0.38; 95% confidence interval, 0.29–0.50).

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