ClinVar Miner

Submissions for variant NM_024079.5(ALG8):c.174+30del

dbSNP: rs59662312
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001549110 SCV001769199 benign ALG8 congenital disorder of glycosylation 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001595106 SCV001828093 benign not provided 2019-09-02 criteria provided, single submitter clinical testing

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