ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.1218del (p.His407fs)

dbSNP: rs727504226
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000723891 SCV000203822 pathogenic not provided 2014-01-22 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory, Children's Mercy Hospital and Clinics RCV000154156 SCV000221258 pathogenic Mowat-Wilson syndrome 2015-03-02 no assertion criteria provided clinical testing

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