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. 2023 Oct 6;11:1248733. doi: 10.3389/fped.2023.1248733

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© 2023 Cason, Chambers, Tu, Chryst-Stangl, Huggins, Lane, Ochoa, Jackson and Gbadegesin.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Flow diagram demonstrating exclusion of patients with missing phenotype^a and genotype* data for the known SSNS risk alleles (termed “missingness”, based on significantly different AF for each comparison group) for variant burden analysis. Number of patients excluded due to missingness: 113 patients with SRNS and 47 patients with SSNS.