ClinVar Miner

List of variants reported as uncertain significance for ALG1-congenital disorder of glycosylation by Revvity Omics, Revvity

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_019109.5(ALG1):c.827G>A (p.Arg276Gln)	rs201975029	0.00045
NM_019109.5(ALG1):c.965A>G (p.Lys322Arg)	rs145851409	0.00007
NM_019109.5(ALG1):c.679C>G (p.Leu227Val)

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