ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.593-9C>T

dbSNP: rs372216323
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001088329 SCV000641889 likely benign Mowat-Wilson syndrome 2024-01-29 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000714224 SCV000844918 likely benign not provided 2018-06-27 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001088329 SCV002799434 likely benign Mowat-Wilson syndrome 2022-05-18 criteria provided, single submitter clinical testing

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