ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.7730-3C>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV002466785 SCV002761417 uncertain significance von Willebrand disease type 2 2019-12-30 criteria provided, single submitter clinical testing

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