Barely Significant
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WWP1 germline variants are associated with normocephalic autism spectrum disorder.

Cell Death Dis · 2020 · PMC7376150 · PMID 32699206

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closest p · 0.0× alpha
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The sentences

highly significantp < 0.00001actually significant
= 0.0252) from the 198 unrelated individuals with ASD/ID (Table 1 ) which is a highly significant difference from European population frequencies from GnomAD ( p < 0.00001; OR = 30.6 with 95% CI 16.27 and 57.59).

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