List of variants reported as benign for ALG11-congenital disorder of glycosylation by Illumina Laboratory Services, Illumina

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_021645.6(UTP14C):c.254G>T (p.Gly85Val)	rs3742289	0.63014
NM_021645.6(UTP14C):c.835C>T (p.Leu279=)	rs3742291	0.56764
NM_021645.6(UTP14C):c.-22A>C	rs3825528	0.40130
NM_021645.6(UTP14C):c.301A>G (p.Thr101Ala)	rs3742290	0.10387
NM_001004127.3(ALG11):c.933G>A (p.Pro311=)	rs61958802	0.03255
NM_001004127.3(ALG11):c.323A>G (p.Asn108Ser)	rs17480245	0.01560
NM_001004127.3(ALG11):c.1107T>C (p.Tyr369=)	rs146432805	0.00031

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