ClinVar Miner

Submissions for variant NM_004562.3(PRKN):c.*887_*890del

dbSNP: rs572345942
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000383992 SCV000461674 uncertain significance Juvenile-onset Parkinson disease 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004695915 SCV005189341 uncertain significance not provided criteria provided, single submitter not provided

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