ClinVar Miner

Submissions for variant NM_031443.4(CCM2):c.803+17C>G

gnomAD frequency: 0.00106  dbSNP: rs374335278
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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 RCV002162964 SCV002414268 benign Cerebral cavernous malformation 2 2023-10-19 criteria provided, single submitter clinical testing

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