ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.2546+25C>T

gnomAD frequency: 0.70354  dbSNP: rs216325
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251920 SCV000305292 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001610583 SCV000605587 benign not provided 2020-04-06 criteria provided, single submitter clinical testing
GeneDx RCV001610583 SCV001834015 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243970 SCV002514656 benign von Willebrand disease type 1 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243971 SCV002514657 benign von Willebrand disease type 3 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243972 SCV002514658 benign von Willebrand disease type 2 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001610583 SCV005236794 benign not provided criteria provided, single submitter not provided

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