ClinVar Miner

Submissions for variant NM_022095.4(ZNF335):c.3820-7_3820-6del

dbSNP: rs150750750
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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 RCV000504231 SCV000598056 likely benign not specified 2015-09-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000903824 SCV001048308 benign not provided 2024-12-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002244977 SCV002514172 benign Microcephalic primordial dwarfism due to ZNF335 deficiency 2021-12-05 criteria provided, single submitter clinical testing

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