ClinVar Miner

Submissions for variant NM_000552.4(VWF):c.5312-19A>C (rs200237834)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV000994805 SCV001148575 uncertain significance not provided 2018-05-01 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001287491 SCV001474186 likely benign none provided 2020-07-09 criteria provided, single submitter clinical testing

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