ClinVar Miner

Submissions for variant NM_000552.4(VWF):c.3258C>T (p.Tyr1086=) (rs112634786)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000243415 SCV000305296 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000280629 SCV000380618 likely benign von Willebrand disorder 2016-06-14 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000755443 SCV000605580 benign not provided 2017-06-09 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000755443 SCV000889902 benign not provided 2018-05-24 criteria provided, single submitter clinical testing
Invitae RCV000755443 SCV001101633 benign not provided 2017-05-11 criteria provided, single submitter clinical testing

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