ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.194-17T>G

gnomAD frequency: 0.00032  dbSNP: rs372128441
Minimum review status: Collection method:
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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 RCV002113065 SCV002398957 benign Juvenile onset Parkinson disease 19A 2024-01-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715594 SCV005287354 benign not provided criteria provided, single submitter not provided

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