ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.3222+31C>T

gnomAD frequency: 0.29425  dbSNP: rs73051263
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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 RCV000246833 SCV000305294 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001812681 SCV000605572 benign not provided 2020-03-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243973 SCV002514643 benign von Willebrand disease type 1 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243974 SCV002514644 benign von Willebrand disease type 3 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243975 SCV002514645 benign von Willebrand disease type 2 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001812681 SCV005236791 benign not provided criteria provided, single submitter not provided

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