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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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Risk loci burden for patients with SSNS vs. SRNS. NS patients with ≥7 risk alleles have significantly increased odds of developing SRNS (OR 7.4, 95% CI 4.6–12.0; p = 8.2 × 10⁻¹⁶). Note, there were no patients with 12 alleles.