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. 2024 Jul 17;14(7):230419. doi: 10.1098/rsob.230419

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© 2024 The Authors.

Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.

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Figure 1. — Manhattan plot of SAP genome-wide association study. The −log₁₀(p-value) of genetic variants is shown on the y-axis and GRCh37 base pair position within chromosomes on the x-axis. The horizontal dashed line is at p-value 5.8 × 10⁻⁸. The lead variants are labelled with the putative causal genes assigned by V2G.