Barely Significant
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Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.

PLoS Genet · 2011 · PMC3116911 · PMID 21698135

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The sentences

highly significantP = 3.97×10 −7actually significant
Combining the data from all cohorts (1232 patients and 5930 controls) resulted in a highly significant association between TAAD and duplications of 16p13.1 ( P = 3.97×10 −7 , OR = 12.6, 95% CI = 4.2–45.3).

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