ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.8616+43G>C

dbSNP: rs74481153
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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 RCV000253001 SCV000305052 benign not specified 2013-10-28 criteria provided, single submitter clinical testing
GeneDx RCV001569682 SCV001793809 likely benign not provided 2018-07-09 criteria provided, single submitter clinical testing

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