ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.3067+8T>A

dbSNP: rs1573713416
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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 RCV001419878 SCV001622145 likely benign Mowat-Wilson syndrome 2020-09-23 criteria provided, single submitter clinical testing

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