ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.2463C>T (p.Asn821=)

gnomAD frequency: 0.00009  dbSNP: rs193114909
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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 RCV002134694 SCV002413713 likely benign Juvenile onset Parkinson disease 19A 2023-10-20 criteria provided, single submitter clinical testing

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