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. 2023 Feb 2;29(2):483–492. doi: 10.1038/s41591-022-02194-3

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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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Extended Data Fig. 5 — a, Distribution of pathogenic (P), likely pathogenic (LP), uncertain significance (VUS), likely benign (LB) and benign (B) variants across genes among all rare variants detected in known POI genes. b, Distribution of LoF, missense and other types (including in-frame indels and splice region) of all detected variants across genes. c, Distribution of LoF, missense and other types of P/LP variants across genes.