ClinVar Miner

Submissions for variant NM_000552.4(VWF):c.3686T>G (p.Val1229Gly) (rs61749367)

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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 RCV000250437 SCV000305306 likely benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000086670 SCV000884881 benign not provided 2017-08-18 criteria provided, single submitter clinical testing
NIHR Bioresource Rare Diseases, University of Cambridge RCV000851979 SCV000899691 uncertain significance Abnormality of coagulation 2019-02-01 criteria provided, single submitter research
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000250437 SCV001469943 benign not specified 2020-04-30 criteria provided, single submitter clinical testing
Academic Unit of Haematology, University of Sheffield RCV000086670 SCV000118874 not provided not provided no assertion provided not provided

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