ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.13515-7C>T

dbSNP: rs780441103
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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 RCV003757053 SCV004559547 likely benign RYR1-related disorder 2024-02-26 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004005895 SCV004827403 likely benign Malignant hyperthermia, susceptibility to, 1 2023-08-08 criteria provided, single submitter clinical testing

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