ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.1755T>C (p.Phe585=)

gnomAD frequency: 0.00001  dbSNP: rs1412214392
Minimum review status: Collection method:
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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 RCV002155693 SCV002461237 likely benign Juvenile onset Parkinson disease 19A 2022-03-08 criteria provided, single submitter clinical testing

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