ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.2838C>T (p.Tyr946=)

gnomAD frequency: 0.00005  dbSNP: rs148209150
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000537857 SCV000654696 likely benign Juvenile onset Parkinson disease 19A 2022-09-10 criteria provided, single submitter clinical testing

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