ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.32G>A (p.Arg11Gln)

dbSNP: rs1476193985
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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 RCV002128520 SCV002460459 benign Mowat-Wilson syndrome 2022-12-15 criteria provided, single submitter clinical testing

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