ClinVar Miner

Submissions for variant NM_145239.3(PRRT2):c.648C>G (p.Pro216=) (rs772805935)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000866552 SCV001007664 likely benign not provided 2018-12-14 criteria provided, single submitter clinical testing
Invitae RCV001461188 SCV001665074 likely benign Paroxysmal kinesigenic dyskinesia 2020-01-27 criteria provided, single submitter clinical testing

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