ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.216G>A (p.Glu72=)

gnomAD frequency: 0.00013  dbSNP: rs146062011
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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 RCV002158728 SCV002461482 likely benign Juvenile onset Parkinson disease 19A 2021-11-10 criteria provided, single submitter clinical testing

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