ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.666+10C>G

dbSNP: rs373591833
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002083372 SCV002380878 likely benign Juvenile onset Parkinson disease 19A 2021-03-23 criteria provided, single submitter clinical testing

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