Barely Significant
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Association of the MTHFR A1298C variant with unexplained severe male infertility.

PLoS One · 2012 · PMC3311580 · PMID 22457816

Europe PMCDOI
1
hedged sentence
0.0308
closest p · 0.6× alpha
0.0308
boldest claim

The sentences

slightly significantp = 0.03078actually significant
The haplotype CCAA showed a slightly significant difference (p = 0.03078) between controls and all infertile patients (OR = 1.389, 95% CI = 1.039–1.855), and the haplotype CCCC showed statistically significant frequencies between the control group and a combination of all patients (OR = 3.313, 95% CI = 1.488–7.659; p = 0.003880), between control and severe oligozoospermia group (OR = 6.687, 95% CI = 2.461–17.72; p = 0.0000449) and between controls and all azoospermia, severe oligozoospermia and oligozoospermia group respectively (OR = 3.326, 95% CI = 1.4–8.035; p = 0.007307).

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