Barely Significant
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Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.

Nat Genet · 2016 · PMC5086090 · PMID 27723758

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highly significantno p-value reported
This analysis was conducted genome-wide, and then repeated with the exclusion of the MHC region (chr6: 24–36 Mb) due to the extensive LD and highly significant variants in this region.

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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.