ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.696C>T (p.Tyr232=)

dbSNP: rs1060503990
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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 RCV001475926 SCV001680126 likely benign Mowat-Wilson syndrome 2016-09-20 criteria provided, single submitter clinical testing

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