Barely Significant
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Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants.

Heart · 2010 · PMC2976076 · PMID 20937753

Europe PMCDOI
1
hedged sentence
0.0160
closest p · 0.3× alpha
0.0160
boldest claim

The sentences

borderline significantp=0.016actually significant
Three SNPs (rs739374, rs6518580 and rs5993820) showed borderline significant association (p=0.016–0.025) with TOF in 356 cases.

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