ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.1470C>T (p.His490=)

dbSNP: rs767360787
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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 RCV000940873 SCV001086742 likely benign Mowat-Wilson syndrome 2022-11-01 criteria provided, single submitter clinical testing

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