ClinVar Miner

Submissions for variant NM_000552.4(VWF):c.6554G>A (p.Arg2185Gln) (rs2229446)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000241790 SCV000305327 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000401548 SCV000380577 likely benign von Willebrand disorder 2016-06-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000086855 SCV000889928 benign not provided 2018-04-20 criteria provided, single submitter clinical testing
Academic Unit of Haematology, University of Sheffield RCV000086855 SCV000119061 not provided not provided no assertion provided not provided

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