ClinVar Miner

Submissions for variant NM_145239.3(PRRT2):c.649C>A (p.Arg217=)

dbSNP: rs77838305
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001370790 SCV001567326 likely benign Episodic kinesigenic dyskinesia 2023-07-07 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003132480 SCV003812388 uncertain significance not provided 2021-03-24 criteria provided, single submitter clinical testing

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