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. 2023 May 17;618(7966):774–781. doi: 10.1038/s41586-023-06079-4

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — a, Variation of height phenotype, PGS estimates and accuracy across different GD bins in ATLAS. b, Variation of log neutrophil count phenotype, PGS estimates and accuracy across different GD bins in ATLAS. The 36,778 ATLAS individuals are divided into 20 equal-interval GD bins. Bins with fewer than 50 individuals are not shown owing to large s.e.m. All panels share the same layout: the x axis is the average GD within the bin; the y axis is the average phenotype (top), PGS (middle) and individual PGS accuracy (bottom); the error bars represent ±1.96 s.e.m.