Barely Significant
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Genetic association of -1562C>T polymorphism in the MMP9 gene with primary glaucoma in a north Indian population.

PLoS One · 2018 · PMC5809065 · PMID 29432439

3
hedged sentences
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

close to significancep = 0.050actually significant
The difference in genotypic distribution between POAG males and control male subjects was close to significance threshold (p = 0.050).

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borderline significanceno p-value reported
-1562C>T MMP9 polymorphism revealed borderline significance with POAG The prevalence of CC genotype was greater in controls (69.75%) than in cases (61.16%) while frequency of CT genotype was found to be higher in cases (37.94%) as compared to the control group (28.61%).

also in 7,017 other papers

highly significantno p-value reported
In a Taiwanese population, highly significant association was observed between PACG and a non synonymous SNP in exon 6 of the MMP9 gene (rs2664538; now merged into rs17576) [ 35 ].

also in 132,142 other papers

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.