ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.1266A>T (p.Leu422=)

gnomAD frequency: 0.00078  dbSNP: rs61758427
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 RCV002064765 SCV002406828 benign Juvenile onset Parkinson disease 19A 2021-08-29 criteria provided, single submitter clinical testing

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