Association of SLCO1B1 genetic variants with neonatal hyperbilirubinemia: a consolidated analysis of 36 studies.

BMC Pediatr · 2025 · PMC11951654 · PMID 40155882

Europe PMC DOI

hedged sentence

0.0660

closest p · 1.3× alpha

0.0660

boldest claim

The sentences

approached significanceP = 0.066so close (0.05 < p ≤ 0.1)

AA approached significance (OR: 1.296; P = 0.066), pointing toward a possible risk connected to the G allele among Chinese neonates.

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