ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.9G>A (p.Gln3=)

dbSNP: rs149882004
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000148009 SCV000195508 uncertain significance Mowat-Wilson syndrome 2014-06-26 criteria provided, single submitter clinical testing
GeneDx RCV000727130 SCV000520108 benign not provided 2021-03-09 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000727130 SCV000706023 uncertain significance not provided 2017-02-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000148009 SCV000763936 benign Mowat-Wilson syndrome 2024-01-27 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000148009 SCV002045618 benign Mowat-Wilson syndrome 2021-11-07 criteria provided, single submitter clinical testing

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