ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.3384G>A (p.Glu1128=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002621708 SCV002965257 likely benign Mowat-Wilson syndrome 2022-08-15 criteria provided, single submitter clinical testing

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