ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.1347A>G (p.Pro449=)

dbSNP: rs777389017
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002150609 SCV002458864 likely benign Glycogen storage disease type III 2023-08-11 criteria provided, single submitter clinical testing

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