ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.2331C>T (p.Gly777=)

gnomAD frequency: 0.00003  dbSNP: rs370155769
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002205585 SCV002369774 benign Juvenile onset Parkinson disease 19A 2022-05-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715590 SCV005287376 benign not provided criteria provided, single submitter not provided

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