ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.194-5G>T

gnomAD frequency: 0.00359  dbSNP: rs753576283
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000560357 SCV000654692 likely benign Juvenile onset Parkinson disease 19A 2023-01-24 criteria provided, single submitter clinical testing
GeneDx RCV001550927 SCV001771333 likely benign not provided 2020-10-25 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000560357 SCV004049370 likely benign Juvenile onset Parkinson disease 19A 2023-04-11 criteria provided, single submitter clinical testing

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