ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.1424-44A>G (rs2291638)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000252556 SCV000305378 benign not specified criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001549087 SCV001769169 benign Glycogen storage disease type III 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001618395 SCV001845612 benign not provided 2018-06-23 criteria provided, single submitter clinical testing

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