ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.3196C>T (p.His1066Tyr)

dbSNP: rs1703134304
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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 RCV001038898 SCV001202398 uncertain significance Mowat-Wilson syndrome 2021-08-31 criteria provided, single submitter clinical testing

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