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. 2023 Nov 11;14:7300. doi: 10.1038/s41467-023-43036-1

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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. 2 — A A forest plot depicting the association details for HLA-B top risk variant rs543685299 in each of the eight cohorts tested and including all ancestries. B A forest plot depicting the association details for the top ERAP1 protective intronic variant rs3198304 in the eight cohorts tested and including all ancestries. A meta-analysis result combining all cohorts is the lowest row (bold), meta-analysis OR is presented by a red diamond. Center points represent odds ratios as estimated by approximate Firth logistic regression, with errors bars representing 95% confidence intervals. P values are uncorrected and reflect two-sided tests. Numbers below the cases and controls columns represent counts of individuals with homozygote reference, heterozygote and homozygous alternative genotypes, respectively.