ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.466C>T (p.Arg156Cys)

gnomAD frequency: 0.00004  dbSNP: rs147021269
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502069 SCV000598032 likely benign not specified 2016-12-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000812201 SCV000952506 likely benign Mowat-Wilson syndrome 2024-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000812201 SCV002045605 uncertain significance Mowat-Wilson syndrome 2021-11-07 criteria provided, single submitter clinical testing

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