Barely Significant
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"Desert" gene (Chr9p21) variants as novel markers for coronary artery disease.

Anatol J Cardiol · 2017 · PMC5731273 · PMID 28559532

1
hedged sentence
0.0010
closest p · 0.0× alpha
0.0010
boldest claim

The sentences

highly significantp=0.001actually significant
rs2383206 Similar to the SNP rs10757278, the genetic variations of rs2383206 among studied groups were found to be highly significant (p=0.001).

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