ClinVar Miner

Submissions for variant NM_000642.3(AGL):c.2950-21T>A (rs2035961)

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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 RCV000249993 SCV000305389 benign not specified criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001549088 SCV001769172 benign Glycogen storage disease type III 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001610584 SCV001841535 benign not provided 2018-06-23 criteria provided, single submitter clinical testing

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