Barely Significant
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Effect of the rs2259816 polymorphism in the HNF1A gene on circulating levels of c-reactive protein and coronary artery disease (the ludwigshafen risk and cardiovascular health study).

BMC Med Genet · 2010 · PMC2994837 · PMID 21062467

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highly significantno p-value reported
For the rs2259816 polymorphism we found a highly significant association with circulating levels of CRP confirming other reports.

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The odds ratio for coronary artery disease was only very slightly increased in carriers of the A-allele and this association did not reach statistical significance.

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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.