ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.1754del (p.Phe585fs)

dbSNP: rs786204809
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, Children's Mercy Hospital and Clinics RCV000169708 SCV000221246 pathogenic Mowat-Wilson syndrome 2015-03-02 no assertion criteria provided clinical testing

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