Significant Associations between AXIN1 rs1805105, rs12921862, rs370681 Haplotypes and Variant Genotypes of AXIN2 rs2240308 with Risk of Congenital Heart Defects.

Int J Environ Res Public Health · 2020 · PMC7589771 · PMID 33096676

Europe PMC DOI

hedged sentence

0.0480

closest p · 1.0× alpha

0.0480

boldest claim

The sentences

marginally significantp = 0.048actually significant

Moreover, there was a marginally significant unadjusted effect of AXIN1 rs1805105 variant in the recessive gene model ( p = 0.048, OR = 0.51, 95% CI: 0.25–1.01) and after adjusting for maternal age group, AXIN1 rs1805105 gene variant was significantly associated with increased odds of ASD ( p = 0.041, adjusted OR = 0.48, 95% CI: 0.24–0.99).

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