ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.2647G>A (p.Val883Met)

gnomAD frequency: 0.00004  dbSNP: rs550047043
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000797909 SCV000937495 likely benign Mowat-Wilson syndrome 2024-01-08 criteria provided, single submitter clinical testing
GeneDx RCV001592980 SCV001826797 likely benign not provided 2020-12-28 criteria provided, single submitter clinical testing

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