Identifying rare variants associated with hypertension using the C-alpha test.

BMC Proc · 2014 · PMC4143634 · PMID 25519391

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nominally significantno p-value reported

Results A total of 408,343 CVs were analyzed; 13,017 were nominally significant ( p value for association test <0.05), and approximately 1% were located in genes.

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highly significantno p-value reported

We identified highly significant common variants within chromosome 3, as well as rare variants around these locations.

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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.