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. 2020 Oct 9;22(10):e19040. doi: 10.2196/19040

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©Alejandro Mendoza-Alvarez, Adrián Muñoz-Barrera, Luis Alberto Rubio-Rodríguez, Itahisa Marcelino-Rodriguez, Almudena Corrales, Antonio Iñigo-Campos, Ariel Callero, Eva Perez-Rodriguez, Jose Carlos Garcia-Robaina, Rafaela González-Montelongo, Jose Miguel Lorenzo-Salazar, Carlos Flores. Originally published in the Journal of Medical Internet Research (http://www.jmir.org), 09.10.2020.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research, is properly cited. The complete bibliographic information, a link to the original publication on http://www.jmir.org/, as well as this copyright and license information must be included.

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Selected snapshots of the HADA graphical interface with step-by-step instructions. Users can query variants of interest or alternatively upload an individual variant calling file (VCF) in the home page (A). The detected variants tab (B) shows the existence of variants affecting function in the query, as well as other variants in hereditary angioedema (HAE) genes. Plots are also generated and available for users to download (C).