ClinVar Miner

Submissions for variant NM_000540.2(RYR1):c.6272C>A (p.Pro2091His) (rs1555781055)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000660420 SCV000782507 uncertain significance Central core myopathy 2016-11-04 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000721602 SCV000852699 uncertain significance not provided 2013-10-23 criteria provided, single submitter clinical testing

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