ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.73+1del

dbSNP: rs786204813
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000224619 SCV000280730 pathogenic not provided 2015-06-05 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory, Children's Mercy Hospital and Clinics RCV000169713 SCV000221252 pathogenic Mowat-Wilson syndrome 2015-03-02 no assertion criteria provided clinical testing

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