ClinVar Miner

Submissions for variant NM_000552.4(VWF):c.3719C>T (p.Pro1240Leu) (rs150576611)

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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 RCV000327886 SCV000380607 uncertain significance von Willebrand disorder 2016-06-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001284371 SCV001470124 uncertain significance not provided 2019-12-17 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001285695 SCV001472170 likely benign none provided 2019-09-05 criteria provided, single submitter clinical testing

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