ClinVar Miner

Submissions for variant NM_000552.5(VWF):c.5520dup (p.Gly1841fs)

dbSNP: rs1591858979
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City RCV000985056 SCV001132997 likely pathogenic von Willebrand disease type 1 2019-08-25 no assertion criteria provided clinical testing

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