ClinVar Miner

Submissions for variant NM_007217.4(PDCD10):c.475-4del

dbSNP: rs772163237
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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 RCV001488704 SCV001693227 likely benign Cerebral cavernous malformation 3 2023-03-01 criteria provided, single submitter clinical testing

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