ClinVar Miner

Submissions for variant NM_003690.5(PRKRA):c.784+15del

dbSNP: rs200581051
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002083090 SCV002371460 benign Dystonia 16 2023-11-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002083090 SCV002802763 likely benign Dystonia 16 2021-09-19 criteria provided, single submitter clinical testing

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