ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.750A>T (p.Arg250=)

dbSNP: rs2101597985
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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 RCV001398074 SCV001599840 likely benign Juvenile onset Parkinson disease 19A 2019-02-21 criteria provided, single submitter clinical testing

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