ClinVar Miner

Submissions for variant NM_003690.5(PRKRA):c.515-11del

dbSNP: rs199996045
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000395086 SCV000419679 likely benign Dystonic disorder 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001555781 SCV001777248 likely benign not provided 2022-03-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002057612 SCV002473235 benign Dystonia 16 2025-01-06 criteria provided, single submitter clinical testing

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