ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.309A>G (p.Leu103=)

gnomAD frequency: 0.00002  dbSNP: rs187331667
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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 RCV000501819 SCV000598023 uncertain significance not specified 2015-09-08 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001815339 SCV002063896 likely benign not provided 2021-11-01 criteria provided, single submitter clinical testing
Invitae RCV002056889 SCV002472761 likely benign Mowat-Wilson syndrome 2023-08-04 criteria provided, single submitter clinical testing

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