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. 2023 Oct 31;14:6934. doi: 10.1038/s41467-023-42532-8

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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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Fig. 5 — Variant ids are defined as rsid-risk-increasing allele. Included are species that reach the multiple testing-corrected threshold of 7.352941e-10 for at least one of the variants. Associations reaching the genome-wide-significant (P < 5e-8) or the multiple testing-corrected threshold are indicated by one or two asterisks, respectively. Colored effect estimates are shown for the associations reaching nominal significance corrected for the number of PCs explaining 90% of the variance (P < 7.352941e-4). Two-sided P-values for lipid species were calculated using a linear-mixed-model.