ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.234G>C (p.Leu78=)

dbSNP: rs1413136303
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002170678 SCV002348717 likely benign Mowat-Wilson syndrome 2022-02-10 criteria provided, single submitter clinical testing

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