ClinVar Miner

Submissions for variant NM_000552.4(VWF):c.4304A>G (p.Asn1435Ser) (rs11063987)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000302817 SCV000380598 likely benign von Willebrand disorder 2016-06-14 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001000040 SCV000884878 benign not specified 2018-08-24 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000756904 SCV000888700 benign not provided 2018-06-18 criteria provided, single submitter clinical testing

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