ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.897C>G (p.Pro299=)

gnomAD frequency: 0.00001  dbSNP: rs371261372
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002219154 SCV002377119 likely benign Juvenile onset Parkinson disease 19A 2021-10-26 criteria provided, single submitter clinical testing

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