ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.882A>G (p.Lys294=)

gnomAD frequency: 0.00001  dbSNP: rs1028503337
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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 RCV002167048 SCV002332288 likely benign Mowat-Wilson syndrome 2024-06-15 criteria provided, single submitter clinical testing

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