ClinVar Miner

Submissions for variant NM_022095.4(ZNF335):c.3354C>T (p.Leu1118=)

gnomAD frequency: 0.01110  dbSNP: rs35156034
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000960315 SCV001107280 benign not provided 2025-01-19 criteria provided, single submitter clinical testing
GeneDx RCV000960315 SCV001865737 benign not provided 2020-04-07 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002245785 SCV002514183 benign Microcephalic primordial dwarfism due to ZNF335 deficiency 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000960315 SCV005313854 benign not provided criteria provided, single submitter not provided

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