ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.7790T>A (p.Ile2597Asn)

dbSNP: rs886049737
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000393200 SCV000380554 uncertain significance Hereditary von Willebrand disease 2016-06-14 criteria provided, single submitter clinical testing

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