ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.193C>T (p.Leu65=)

dbSNP: rs772086117
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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 RCV002089477 SCV002328890 likely benign Glycogen storage disease type III 2021-09-24 criteria provided, single submitter clinical testing

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