ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.4621-34C>T

gnomAD frequency: 0.00879  dbSNP: rs114935281
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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 RCV000244430 SCV000304941 benign not specified 2013-10-22 criteria provided, single submitter clinical testing
GeneDx RCV001589242 SCV001815598 likely benign not provided 2018-07-06 criteria provided, single submitter clinical testing

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