ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.194-21G>T

gnomAD frequency: 0.58031  dbSNP: rs2296478
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001668987 SCV001882719 benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073123 SCV002406900 benign Juvenile onset Parkinson disease 19A 2024-01-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002073123 SCV004049364 benign Juvenile onset Parkinson disease 19A 2023-04-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001668987 SCV005287352 benign not provided criteria provided, single submitter not provided

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