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Fig. 1 | BMC Genomic Data

Fig. 1

From: The global carrier frequency and genetic prevalence of Upshaw-Schulman syndrome

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

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