ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.1533G>A (p.Glu511=)

gnomAD frequency: 0.00002  dbSNP: rs773744229
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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 RCV002194132 SCV002486627 likely benign Juvenile onset Parkinson disease 19A 2022-08-09 criteria provided, single submitter clinical testing

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