ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.12415G>A (p.Gly4139Ser)

dbSNP: rs1489505433
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000721271 SCV000852295 uncertain significance not provided 2016-07-25 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000721271 SCV003812461 uncertain significance not provided 2022-01-25 criteria provided, single submitter clinical testing

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