ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.2804T>C (p.Met935Thr)

gnomAD frequency: 0.00001  dbSNP: rs201902790
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000863246 SCV001003875 benign Mowat-Wilson syndrome 2024-01-19 criteria provided, single submitter clinical testing
GeneDx RCV001556101 SCV001777620 likely benign not provided 2020-12-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000863246 SCV002045665 benign Mowat-Wilson syndrome 2021-11-07 criteria provided, single submitter clinical testing

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