ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.4625A>G (p.Tyr1542Cys)

dbSNP: rs2136412168
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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 RCV002264863 SCV002546322 likely pathogenic von Willebrand disease type 2 2020-12-10 criteria provided, single submitter research

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