ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.2158-4T>G

dbSNP: rs2100760100
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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 RCV001403134 SCV001604995 likely benign Glycogen storage disease type III 2020-07-21 criteria provided, single submitter clinical testing

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