ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.10118T>G (p.Val3373Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV002776566 SCV003035485 uncertain significance Malignant hyperthermia, susceptibility to, 1 2022-07-06 criteria provided, single submitter clinical testing

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