ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.747G>A (p.Thr249=)

dbSNP: rs587784569
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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 RCV000148004 SCV000195502 uncertain significance Mowat-Wilson syndrome 2013-06-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000148004 SCV005741252 likely benign Mowat-Wilson syndrome 2024-03-23 criteria provided, single submitter clinical testing

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