ClinVar Miner

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

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003120234 SCV003800173 benign Cerebral cavernous malformation 2 2022-07-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003120234 SCV004538440 benign Cerebral cavernous malformation 2 2023-03-21 criteria provided, single submitter clinical testing

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