ClinVar Miner

Submissions for variant NM_000552.4(VWF):c.1728G>T (p.Met576Ile) (rs150146744)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000343818 SCV000380639 likely benign von Willebrand disorder 2016-06-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000506040 SCV000602289 likely benign not specified 2017-03-22 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000506040 SCV000605570 likely benign not specified 2016-10-25 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000086574 SCV000888674 likely benign not provided 2017-03-22 criteria provided, single submitter clinical testing
Academic Unit of Haematology, University of Sheffield RCV000086574 SCV000118778 not provided not provided no assertion provided not provided

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