ClinVar Miner

Submissions for variant NM_000552.4(VWF):c.390C>T (p.Ser130=) (rs2229444)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000241934 SCV000305310 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000291556 SCV000380655 likely benign von Willebrand disorder 2016-06-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000760122 SCV000889911 benign not provided 2018-05-11 criteria provided, single submitter clinical testing

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