ClinVar Miner

Submissions for variant NM_021957.4(GYS2):c.1422+23C>G (rs7977474)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000244570 SCV000313843 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000675352 SCV001842008 benign not provided 2018-06-29 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001702402 SCV001934069 benign Glycogen storage disease due to hepatic glycogen synthase deficiency 2021-08-10 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories,Mayo Clinic RCV000675352 SCV000801018 benign not provided 2015-10-23 no assertion criteria provided clinical testing

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