ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.10884C>G (p.Arg3628=)

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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 RCV005185164 SCV005820196 likely benign RYR1-related disorder 2024-02-23 criteria provided, single submitter clinical testing

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