COMT genetic variation confers risk for psychotic and affective disorders: a case control study.

Behav Brain Funct · 2005 · PMC1282571 · PMID 16232322

Europe PMC DOI

hedged sentences

0.0620

closest p · 1.2× alpha

0.0620

boldest claim

The sentences

showed a trendp = 0.062so close (0.05 < p ≤ 0.1)

The A allele of SNP -278A/G showed a trend for significance in this group (p = 0.062; OR = 1.34).

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highly significantno p-value reported

saw an association of the Valine allele in their cohort, its moderate effect combined with highly significant p-values for two SNPs located in intron 1 and the 3'UTR (rs737865 and rs165599) has led to the hypothesis that the Val/Met variant may not contribute to disease but may simply be in strong LD with the actual, as of yet unidentified pre-disposing variant [ 40 ].

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.