IDO1 and IDO2 non-synonymous gene variants: correlation with crohn's disease risk and clinical phenotype.

PLoS One · 2014 · PMC4277413 · PMID 25541686

Europe PMC DOI

hedged sentence

0.0570

closest p · 1.1× alpha

0.0570

boldest claim

The sentences

nearly reached significanceP = 0.057so close (0.05 < p ≤ 0.1)

All patients with the 7CA gene variant demonstrated homozygosity for the variant allele, a finding which nearly reached significance (non-IBD 0/674 vs CD 8/1220; P = 0.057).

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