ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.194-6del

dbSNP: rs58549467
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001534238 SCV001751144 benign not provided 2019-08-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002071918 SCV002486923 benign Juvenile onset Parkinson disease 19A 2024-01-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002071918 SCV004049366 benign Juvenile onset Parkinson disease 19A 2023-04-11 criteria provided, single submitter clinical testing

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