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. 2024 Nov 6;15:9568. doi: 10.1038/s41467-024-53634-2

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

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Fig. 3 — a Distribution of the rs570516915 G allele frequency and CP prevalence in 19 administrative regions of Finland. The variation in allele frequency and CP prevalence across distinct regions are illustrated by the intensity of the blue shading. Regions are labeled by their corresponding codes from Statistics Finland and shown in Supplementary Data 8. b Correlation between the regional allele frequency of rs570516915 and prevalence of CP. Allele frequency was estimated using birthplace data of 306,678 FinnGen study participants. Regional CP prevalences were estimated using nationwide data on the first recorded addresses and CP related diagnosis codes of 5,216,731 individuals (5162 with CP). Red line represents the ordinary least squares regression line. Pearson’s r and P value (two-sided) shown at the top of the plot indicate the strength and statistical significance of correlation. See Supplementary Data 8 for raw numbers.