Barely Significant
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Admixture-informed polygenic risk reporting using the ePRS framework.

Nat Commun · 2026 · PMC13323344 · PMID 42062286

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highly significantno p-value reported
However, currently, we did not account for linkage disequilibrium between variants in the computation of the variance, and therefore, in primary analysis, we only used PRSs that rely on a limited number of highly significant, independent, trait loci.

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