ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.2904C>T (p.Asp968=)

dbSNP: rs760319249
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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 RCV001438717 SCV001641597 likely benign Glycogen storage disease type III 2022-10-17 criteria provided, single submitter clinical testing

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