ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.2013C>T (p.Ser671=)

gnomAD frequency: 0.00001  dbSNP: rs760022807
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001534367 SCV001751291 likely benign not provided 2020-10-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003611552 SCV004489679 likely benign Mowat-Wilson syndrome 2024-07-15 criteria provided, single submitter clinical testing

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