Association of PRKCQ variants with breast cancer susceptibility and clinicopathological features.

BMC Cancer · 2025 · PMC12210595 · PMID 40597019

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hedged sentence

0.0001

closest p · 0.0× alpha

0.0001

boldest claim

The sentences

highly significantp < 0.0001actually significant

A highly significant association was observed for rs1248923790 ( p < 0.0001, χ2 = 26.39). the TT genotype was significantly more common in disease cases (201) compared to controls (136), with an increased risk of disease (OR = 2.106, RR = 1.446, 95% CI: 1.249–1.679).

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