Fig. 1From: The global carrier frequency and genetic prevalence of Upshaw-Schulman syndromeADAMTS13 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 variantsBack to article page