ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.5318C>G (p.Pro1773Arg)

dbSNP: rs1969269453
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine RCV001258126 SCV001435014 uncertain significance Malignant hyperthermia, susceptibility to, 1 criteria provided, single submitter clinical testing

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