Barely Significant
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Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.

Mol Autism · 2010 · PMC2907567 · PMID 20678243

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1
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0.0200
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0.0200
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nominally significantP = 0.02actually significant
Nominally significant ORs were observed for the risk alleles for EN2 ( P = 0.02), PITX ( P = 0.01) and ATP2B2 ( P = 0.01) (Table 2 ).

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