ClinVar Miner

Submissions for variant NM_022095.4(ZNF335):c.648G>A (p.Pro216=)

gnomAD frequency: 0.00013  dbSNP: rs201180565
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000192308 SCV000249508 uncertain significance not specified 2014-06-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000892123 SCV001035981 likely benign not provided 2023-10-13 criteria provided, single submitter clinical testing

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