ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.808-4A>G

dbSNP: rs759097764
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000193515 SCV000249492 uncertain significance not specified 2015-05-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003765242 SCV004628461 likely benign Mowat-Wilson syndrome 2024-01-24 criteria provided, single submitter clinical testing

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