ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.1182A>C (p.Pro394=)

dbSNP: rs762006325
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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 RCV002208413 SCV002493191 likely benign Mowat-Wilson syndrome 2021-07-14 criteria provided, single submitter clinical testing

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