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. 2023 Oct 20;28(9):4011–4019. doi: 10.1038/s41380-023-02292-9

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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. 4 — Prediction of RTV by polygenic score (PGS) in the African, non-British European, and South Asian ancestry groups from the UK Biobank. The predictive accuracy of the PGS (R²) was assessed in each cohort for a PGS calculated using two methodologies, PRSice and PRS-CS. PRSice PGS were calculated using all single nucleotide polymorphisms surviving LD pruning from the discovery GWAS (p-value threshold of 1). *p < 0.05, ***p < 2.63 × 10^-3.