Estimation and mapping of the missing heritability of human phenotypes.

Nature · 2026 · PMC12851931 · PMID 41225014

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marginally significantno p-value reported

We selected 41 complex phenotypes spanning a wide range of human traits and common diseases (Supplementary Table 3 ) and showing a marginally significant estimate of h PED 2 from 171,446 pairs of relatives in the UKB.

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