ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.13514+10C>G

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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 RCV005165068 SCV005796968 likely benign RYR1-related disorder 2024-02-22 criteria provided, single submitter clinical testing

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