ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.13365G>A (p.Gly4455=)

dbSNP: rs1656511589
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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 RCV002766743 SCV003020082 likely benign RYR1-related disorder 2022-10-05 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004007592 SCV004826207 likely benign Malignant hyperthermia, susceptibility to, 1 2023-05-30 criteria provided, single submitter clinical testing

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