Barely Significant
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Methylomic Changes in MTHFR Promoter Region, along with the Heterozygous C677T Polymorphism, Contribute to the Risk of Thrombotic Stroke.

J Mol Neurosci · 2025 · PMC12279560 · PMID 40691374

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

The sentences

highly significantP = 0.005actually significant
As presented in Table 3 , the allele frequency of MTHFR-C677T showed a highly significant association with stroke cases, with a notable difference in genotype distribution between patients and controls (χ 2 = 7.92, P = 0.005).

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