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. 2021 Nov 17;22:50. doi: 10.1186/s12863-021-01010-0

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — ADAMTS13 gene disease-causing variants and gnomAD allele frequencies. a flow chart of identification and classification of ADAMTS13 disease-causing variants. ADAMTS13 variants were extracted from PubMed & Scopus citations. ADAMTS13 missense, nonsense, frameshift, inframe, splice acceptor / donor variants were collected from HGMD Public (2016 version), ClinVar and gnomAD database. b Venn diagram of mined PubMed & Scopus, HGMD, ClinVar and gnomAD variants. c Venn diagram of mined PubMed & Scopus, HGMD, ClinVar and gnomAD disease-causing variants