ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.708G>A (p.Lys236=)

dbSNP: rs2149879208
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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 RCV002219670 SCV002378417 likely benign Mowat-Wilson syndrome 2023-05-22 criteria provided, single submitter clinical testing

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