ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.1225C>T (p.Leu409=)

dbSNP: rs1454484326
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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 RCV001484072 SCV001688480 likely benign Glycogen storage disease type III 2022-04-30 criteria provided, single submitter clinical testing

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