Barely Significant
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Innovative computational approaches shed light on genetic mechanisms underlying cognitive impairment among children born extremely preterm.

J Neurodev Disord · 2022 · PMC8903548 · PMID 35240980

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hedged sentence
closest p
boldest claim

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highly significantno p-value reported
We can see that in the European population, the lead variant rs11829294 in the TEAD4 region has a number of LD tags (e.g., 21 variants with r 2 ≥ 0.8) and some of them had highly significant p values; by contrast, the lead variant rs79453226 in the STX18 region has fewer LD tags (2 variants with r 2 ≥ 0.8) that showed suggestive association (Fig. 3 a).

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