ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.666C>T (p.Arg222=)

gnomAD frequency: 0.00001  dbSNP: rs146662449
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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 RCV002212571 SCV002367293 likely benign Mowat-Wilson syndrome 2024-07-19 criteria provided, single submitter clinical testing

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