ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.3359_3364delinsTAATG (p.Gly1120fs)

dbSNP: rs398124280
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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) RCV000723581 SCV000113600 pathogenic not provided 2013-02-25 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory, Children's Mercy Hospital and Clinics RCV000081669 SCV000221263 pathogenic Mowat-Wilson syndrome 2015-03-02 no assertion criteria provided clinical testing

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