ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.770_771del (p.Glu257fs)

dbSNP: rs1573721065
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München RCV000995678 SCV001149984 pathogenic Mowat-Wilson syndrome 2018-03-05 criteria provided, single submitter clinical testing

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