ClinVar Miner

Submissions for variant NM_145261.4(DNAJC19):c.210-7T>A

gnomAD frequency: 0.00006  dbSNP: rs779367415
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000875643 SCV001018098 benign 3-methylglutaconic aciduria type 5 2024-12-17 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004800626 SCV005422673 benign not specified 2024-10-20 criteria provided, single submitter clinical testing

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