ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.507A>G (p.Ser169=)

dbSNP: rs2101558882
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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 RCV001474859 SCV001679036 likely benign Juvenile onset Parkinson disease 19A 2019-12-13 criteria provided, single submitter clinical testing

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