Barely Significant
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Development of next generation sequencing panel for UMOD and association with kidney disease.

PLoS One · 2017 · PMC5469457 · PMID 28609449

Europe PMCDOI
2
hedged sentences
0.0800
closest p · 1.6× alpha
0.0800
boldest claim

The sentences

trending towards significancep = 0.08so close (0.05 < p ≤ 0.1)
Four other variants were extracted from the GENIE study, which were trending towards significance at the five percent level (rs191101580, rs187087030, rs8060932, rs8062123); one of these (rs8060932; p = 0.08) was shown to be in LD with another SNP, rs4238595 (r 2 = 0.89), associated with FJHN [ 21 ]. rs13333226 has been previously reported to be associated with reduced urinary uromodulin excret

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a trend towards significanceno p-value reported
Four other variants, extracted from the GENIE study, showed a trend towards significance, (rs191101580, rs187087030, rs8060932, rs8062123), and rs8060932 is in LD with another SNP (rs4238595) associated with FJHN [ 21 ].

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