ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.3780C>G (p.Asp1260Glu)

dbSNP: rs746617954
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000721507 SCV000852585 uncertain significance not provided 2018-05-11 criteria provided, single submitter clinical testing

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