ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.3544del (p.Glu1182fs) (rs786203991)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia	RCV000167553	SCV000218432	pathogenic	not provided	2015-01-30	no assertion criteria provided	clinical testing

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