ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.4162-12G>C

dbSNP: rs755337032
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248332 SCV000305403 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003517157 SCV004280618 likely benign Glycogen storage disease type III 2024-01-08 criteria provided, single submitter clinical testing

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