ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.461-4G>A

gnomAD frequency: 0.00001  dbSNP: rs769201662
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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 RCV001438155 SCV001641024 likely benign Glycogen storage disease type III 2021-12-09 criteria provided, single submitter clinical testing

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