ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.6182del (p.Phe2061fs)

dbSNP: rs61750614
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Academic Unit of Haematology, University of Sheffield RCV000086847 SCV000119053 not provided not provided no assertion provided not provided
Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico RCV001787065 SCV001572716 pathogenic von Willebrand disease type 3 2021-04-12 no assertion criteria provided clinical testing

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