ClinVar Miner

Submissions for variant NM_006245.4(PPP2R5D):c.323-4A>G

dbSNP: rs368528223
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001650649 SCV001870729 benign not provided 2020-02-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001650649 SCV002394543 likely benign not provided 2025-01-14 criteria provided, single submitter clinical testing

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