ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.220G>A (p.Val74Met)

gnomAD frequency: 0.00002  dbSNP: rs767169568
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000504083 SCV000598033 uncertain significance not specified 2017-02-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001235964 SCV001408673 benign Mowat-Wilson syndrome 2023-10-09 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001235964 SCV002045638 uncertain significance Mowat-Wilson syndrome 2021-11-07 criteria provided, single submitter clinical testing

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