ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.1374G>A (p.Thr458=)

gnomAD frequency: 0.00004  dbSNP: rs148673423
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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 RCV000875314 SCV001017622 likely benign Juvenile onset Parkinson disease 19A 2023-10-22 criteria provided, single submitter clinical testing

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