ClinVar Miner

Submissions for variant NM_000552.4(VWF):c.3925A>G (p.Ile1309Val) (rs61749389)

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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 RCV000086706 SCV000118910 not provided not provided no assertion provided not provided
Clinical Molecular Genetics Laboratory,Johns Hopkins All Children's Hospital RCV000678766 SCV000804945 pathogenic von Willebrand disorder 2010-02-11 no assertion criteria provided clinical testing

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