ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.1876G>T (p.Gly626Ter)

dbSNP: rs727504224
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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) RCV000723945 SCV000203820 pathogenic not provided 2014-04-18 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory, Children's Mercy Hospital and Clinics RCV000154154 SCV000221239 pathogenic Mowat-Wilson syndrome 2015-03-02 no assertion criteria provided clinical testing

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