ClinVar Miner

Submissions for variant NM_021957.4(GYS2):c.1890+25del (rs36023861)

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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 RCV000243906 SCV000313849 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001651246 SCV001867196 benign not provided 2018-06-29 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001701910 SCV001934068 benign Glycogen storage disease due to hepatic glycogen synthase deficiency 2021-08-10 criteria provided, single submitter clinical testing

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