Barely Significant
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The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta-analysis.

Am J Med Genet B Neuropsychiatr Genet · 2019 · PMC6767385 · PMID 30474181

Europe PMCDOI
1
hedged sentence
0.0320
closest p · 0.6× alpha
0.0320
boldest claim

The sentences

nominally significantp = .032actually significant
Nevertheless, observing all SNPs' association results of the PGC‐ADHD dataset at the LRP5 gene (Supporting Information Figure S3), a nominally significant signal could be seen in the male/female combined population at rs4988321 ( p = .032), which is in moderate LD with rs3736228 ( D ′ = 1.0, R 2 = 0.227 at CEU; D ′ = 0.967, R 2 = 0.266 at EUR) but not with rs4988319 ( D ′ = 0.219, R 2 = 0.009 at CEU; D ′ = 0.514, R 2 = 0.056 at EUR).

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