ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.996-9T>C

gnomAD frequency: 0.00178  dbSNP: rs187965193
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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 RCV000651849 SCV000773705 benign Juvenile onset Parkinson disease 19A 2023-11-27 criteria provided, single submitter clinical testing

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