ClinVar Miner

Submissions for variant NM_017649.5(CNNM2):c.2058C>T (p.Phe686=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002962594 SCV003285173 likely benign not provided 2024-11-19 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002962594 SCV004010014 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing CNNM2: BP4

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