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. 2024 Nov 13;15:9839. doi: 10.1038/s41467-024-53595-6

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© The Author(s) 2024

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 — The forest plot displays the top risk-conferring and protective HLA allele across all main analyses. The log₁₀ of the odds ratio (OR) from inverse-variance-weighted fixed-effects meta-analysis is indicated as diamonds for each HLA allele and dataset used along with the 95% confidence intervals (error bars). Different P-value significance levels are indicated by asterisks for nominally significant (P < 0.05*), Bonferroni-corrected (P < 3.70e⁻⁴**), and genome-wide (P < 5e⁻⁸***). MG myasthenia gravis; EOMG early-onset myasthenia gravis, LOMG late-onset myasthenia gravis.