ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.4752C>A (p.Tyr1584Ter)

dbSNP: rs1475440343
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Hematology, Radboud University Medical Center RCV002264866 SCV002546329 pathogenic von Willebrand disease type 3 2020-12-10 criteria provided, single submitter research

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