ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.3539-33G>A

gnomAD frequency: 0.04652  dbSNP: rs148995386
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000250783 SCV000305303 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000250783 SCV000605582 benign not specified 2016-11-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243997 SCV002514616 benign von Willebrand disease type 1 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243998 SCV002514617 benign von Willebrand disease type 3 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243999 SCV002514618 benign von Willebrand disease type 2 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706690 SCV005236787 benign not provided criteria provided, single submitter not provided

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