Barely Significant
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A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure.

Hum Reprod Open · 2024 · PMC11645127 · PMID 39678461

1
hedged sentence
0.0049
closest p · 0.1× alpha
0.0049
boldest claim

The sentences

showed a trendP = 4.88E−03actually significant
Additionally, the SHOC1 gene showed a trend for association under a gene-wise framework ( P = 4.88E−03) ( Table 2 and Supplementary Table S9 ).

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