ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.3589-1G>A

dbSNP: rs1289339080
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000665591 SCV000789738 likely pathogenic Glycogen storage disease type III 2017-02-14 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000665591 SCV002023081 pathogenic Glycogen storage disease type III 2020-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000665591 SCV004050055 likely pathogenic Glycogen storage disease type III 2023-04-11 criteria provided, single submitter clinical testing

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