ClinVar Miner

Submissions for variant NM_031443.4(CCM2):c.609+18C>T

dbSNP: rs201140198
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002100740 SCV002389722 likely benign Cerebral cavernous malformation 2 2021-05-20 criteria provided, single submitter clinical testing

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