Correlations between causal effect sizes of proximal SNPs vary with functional annotations and...

TL;DR

Summary:
- This article, published in *Nature Genetics*, details a sophisticated study on the genetic architecture of complex traits, utilizing advanced statistical genomics to map loci associated with specific phenotypes.
- The research provides critical insights into the functional mechanisms of non-coding variants, significantly advancing our understanding of how genotype-to-phenotype mapping influences human health and disease susceptibility.

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