ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.1672+10C>A

dbSNP: rs751878748
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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 RCV001428650 SCV001631352 likely benign RYR1-related disorder 2024-04-24 criteria provided, single submitter clinical testing

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