Barely Significant
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Assessing <i>ST18</i> gene polymorphisms (rs17315309, rs2304365) in Iraqi patients with Pemphigus vulgaris.

J Med Life · 2024 · PMC11080500 · PMID 38737652

1
hedged sentence
0.0050
closest p · 0.1× alpha
0.0050
boldest claim

The sentences

highly significantP = 0.005actually significant
For SNP rs17315309 A/G, the distribution of heterozygous genotypes showed highly significant differences between the patient and healthy groups ( P = 0.005), with the mutant G-allele being significantly more prevalent in patients than in the healthy group ( P = 0.001).

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