ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.2310G>A (p.Ala770=)

gnomAD frequency: 0.00004  dbSNP: rs113490907
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 RCV001472365 SCV001676495 likely benign Juvenile onset Parkinson disease 19A 2018-01-08 criteria provided, single submitter clinical testing

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