ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.198C>T (p.Ala66=)

gnomAD frequency: 0.00030  dbSNP: rs374727491
Minimum review status: Collection method:
Minimum conflict level:
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 RCV003103873 SCV001015971 likely benign Juvenile onset Parkinson disease 19A 2022-03-27 criteria provided, single submitter clinical testing

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