ClinVar Miner

Submissions for variant NM_031443.4(CCM2):c.204+8G>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003322098 SCV004026176 uncertain significance not provided 2023-03-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005102899 SCV005768644 likely benign Cerebral cavernous malformation 2 2024-08-12 criteria provided, single submitter clinical testing

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