ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.6796+9C>T

gnomAD frequency: 0.00001  dbSNP: rs763585200
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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 RCV003084265 SCV003479708 likely benign RYR1-related disorder 2024-03-30 criteria provided, single submitter clinical testing

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