ClinVar Miner

Submissions for variant NM_001256864.2(DNAJC6):c.2025G>A (p.Ser675=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002927539 SCV003259907 benign Juvenile onset Parkinson disease 19A 2024-02-01 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003963427 SCV004784969 likely benign DNAJC6-related disorder 2019-08-23 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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