ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.194-19T>G

gnomAD frequency: 0.57220  dbSNP: rs2296479
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001692835 SCV001909466 benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073233 SCV002375912 benign Juvenile onset Parkinson disease 19A 2024-01-31 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002073233 SCV004049367 benign Juvenile onset Parkinson disease 19A 2023-04-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001692835 SCV005287353 benign not provided criteria provided, single submitter not provided

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