ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.1106T>A (p.Leu369Ter)

dbSNP: rs797046117
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000195002 SCV000249482 pathogenic Mowat-Wilson syndrome 2014-09-24 criteria provided, single submitter clinical testing

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