Barely Significant
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Analysis of LOXL1 gene variants in Japanese patients with branch retinal vein occlusion.

Mol Vis · 2011 · PMC3244486 · PMID 22194657

1
hedged sentence
0.0933
closest p · 1.9× alpha
0.0933
boldest claim

The sentences

borderline significancep=0.0933so close (0.05 < p ≤ 0.1)
Compared to the CT group, the frequencies of the G allele of rs3825942 and the C allele of rs2165241 were higher in the BRVO EX+ groups with borderline significance (p=0.0933 and p=0.0908, respectively), but the allelic and genotypic frequencies did not differ between any pairs of BRVO total or BRVO EX- and the CT group.

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