ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.14803+9T>C

dbSNP: rs774850935
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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 RCV001473211 SCV001677356 likely benign RYR1-related disorder 2024-12-31 criteria provided, single submitter clinical testing

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