ClinVar Miner

Submissions for variant NM_007217.4(PDCD10):c.213C>T (p.Ser71=)

gnomAD frequency: 0.00001  dbSNP: rs201316215
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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 RCV003600392 SCV001096903 likely benign Cerebral cavernous malformation 3 2023-08-09 criteria provided, single submitter clinical testing

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