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. 2021 Feb 24;12:1258. doi: 10.1038/s41467-020-20851-4

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© The Author(s) 2021

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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Fig. 3 — Each dot represents a SNP, the x-axis shows the chromosomes where each SNP is located, and the y-axis shows −log10 P-value of the association of each SNP with POAG in the cross-ancestry meta-analysis (34,179 cases vs. 349,321 controls). The red horizontal line shows the genome-wide significant threshold (P-value = 5e-8; −log10 P-value = 7.30). The nearest gene to the most significant SNP in each locus has been labeled.