P221: Systematic literature review of GLA variants uncovers additional Fabry Disease-causing variants by Jeffrey Bissonnette, Biliana Veleva-Rotse, Joseph Giuliano, Rhea Kerawala, Derek Timm, Natalie Syverud, Amina Kozaric, Mark Kiel

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P307: Smart categories: LLM-based automatic tagging of categorical information in genomic articles outperforms manual curators yielding improved curation efficiency by Brittnee Jones, Angel Morrow, Armina Herić-Hasić, Kelechi Fletcher, Alexis Jimenez, Kiana Roberts, Dan O'Hara, Jonathan Eads, Mark Kiel

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P177: Evaluation of the genotypic and phenotypic spectrum of pediatric ABCC6 deficiency by Marta Bertamino, David Goldberg, M. Zulf Mughal, Y. Joyce Liao, Lisa Pabst, Lisa R. Sun, Katie Swanner, Ruth du Moulin, Jane Beckwell, Amina Kozaric, Mark Kiel, Carlos Ferreira, Shira Ziegler

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P337: Variant classification is negatively impacted by the absence of biochemical data in published patient reports by Jeffrey Bissonnette, Betty Mathias, Melida Mahinic, Ana Gutalj, Rasema Bihorac Hrelja, Mirna Racic, Sabina Alagic, Ena Toman, Paty Romero, Jane Beckwell, Elizabeth Wiley, Kathryn Curry, Anna McGill, Amina Kozaric, Mark Kiel

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P020: Introducing an interactive, searchable database of LC-FAOD gene variants, genotypes and phenotypes by Vanessa Rangel Miller, Omid Japalaghi, Heather Richbourg, Moeenaldeen AlSayed, Peter Baker, II, Sarah C. Grünert, Sean Daugherty, Tali Ekstein, Mark Kiel, Aneal Khan, Hironori Kobayashi, Lawrence Korngut, Stephanie Monteleone, Ida Vanessa Schwartz, Nicole Miller, Jerry Vockley

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