ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.1758T>C (p.Ser586=)

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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 RCV002632835 SCV003510313 likely benign Glycogen storage disease type III 2024-09-12 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV002632835 SCV003820546 uncertain significance Glycogen storage disease type III 2019-10-21 criteria provided, single submitter clinical testing

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