Barely Significant
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Maternal <i>RFC1</i> Gene Polymorphisms and Neural Tube Defects: A Case-Control Study in Ethiopia.

Genes (Basel) · 2026 · PMC13115709 · PMID 42074596

Europe PMCDOI
1
hedged sentence
0.1940
closest p · 3.9× alpha
0.1940
boldest claim

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did not reach statistical significancep = 0.194not close (p > 0.1)
The recessive model analysis (GG versus AA + AG) indicated reduced odds of NTD occurrence among GG carriers, but again this finding did not reach statistical significance (OR = 0.563, 95% CI: 0.236–1.340, p = 0.194).

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