ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.3792A>T (p.Gly1264=) (rs148606237)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000443781 SCV000521515 likely benign not provided 2021-05-24 criteria provided, single submitter clinical testing
Invitae RCV000530507 SCV000626740 benign Glycogen storage disease type III 2020-11-21 criteria provided, single submitter clinical testing

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