ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.14928C>T (p.Phe4976=)

dbSNP: rs368874586
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002177430 SCV002342222 likely benign RYR1-related disorder 2023-12-26 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004011211 SCV004816282 likely benign Malignant hyperthermia, susceptibility to, 1 2023-12-13 criteria provided, single submitter clinical testing

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