Barely Significant
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Hypothesis-free phenotype prediction within a genetics-first framework.

Nat Commun · 2023 · PMC9938118 · PMID 36808136

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highly significantno p-value reported
Evaluation on both cohorts similarly confirms the predictions as highly significant yet also characterises the predictions as having a high false-positive rate; expectations are that for roughly 1/3–1/2 of confirmed high-scoring predictions, the causal genetic explanations will be true.

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