Functional rare variant in a C/EBPbeta binding site in NINJ2 gene increases the risk of coronary artery disease.

Aging (Albany NY) · 2021 · PMC8714150 · PMID 34897030

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highly significantno p-value reported

In the combined population, SNP rs34166160 was found to confer a highly significant risk to CAD ( p -obs = 1.57 × 10 −5 , OR = 3.58).

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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.

Functional rare variant in a <i>C/EBP</i><i>beta</i> binding site in <i>NINJ2</i> gene increases the risk of coronary artery disease.

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