ClinVar Miner

Submissions for variant NM_000153.3(GALC):c.1834+22dup

dbSNP: rs34752717
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000513715 SCV000610505 likely benign not provided 2017-06-12 criteria provided, single submitter clinical testing
GeneDx RCV000513715 SCV001836902 benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001701026 SCV001925549 benign not specified no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001701026 SCV001962781 benign not specified no assertion criteria provided clinical testing

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