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. 2024 Jun 10;56(7):1371–1376. doi: 10.1038/s41588-024-01787-7

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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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Extended Data Fig. 7 — The figure shows the shared haplotype in a ± 250-kb window surrounding the p.S71R variant based on common markers on the Infinium Global Diversity Array-8 (available for 16 out of 18 p.S71R carriers). The y-axis shows SNP IDs with the distance to the p.S71R variant in parentheses, and the x-axis shows the p.S71R genotype (both alleles are shown for the homozygous carrier). The minimal common region extends from -131,546 bp downstream to 182,121 bp upstream of the p.S71R variant.