List of variants in gene DDOST reported as benign for congenital disorder of glycosylation type I

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_005216.5(DDOST):c.646-16C>T	rs607254	0.38527
NM_005216.5(DDOST):c.456+18C>T	rs3738140	0.19425
NM_005216.4(DDOST):c.22G>C (p.Gly8Arg)	rs537816	0.02282
NM_005216.5(DDOST):c.66G>A (p.Ala22=)	rs17837938	0.01665
NM_005216.5(DDOST):c.265+9T>A	rs79243170	0.01029
NM_005216.5(DDOST):c.-12A>C	rs61739382	0.00736
NM_005216.5(DDOST):c.663G>A (p.Gly221=)	rs41307775	0.00625
NM_005216.5(DDOST):c.1176C>T (p.Ser392=)	rs149576051	0.00320
NM_005216.5(DDOST):c.776C>T (p.Ala259Val)	rs138061134	0.00201
NM_005216.5(DDOST):c.353-11G>C	rs202107268	0.00182
NM_005216.5(DDOST):c.1209C>T (p.Arg403=)	rs148883998	0.00148
NM_005216.5(DDOST):c.893G>A (p.Arg298Gln)	rs117925699	0.00098
NM_005216.5(DDOST):c.36C>G (p.Leu12=)	rs143329944	0.00081
NM_005216.5(DDOST):c.1293C>T (p.His431=)	rs117634838	0.00031
NM_005216.5(DDOST):c.1170+16dup	rs566726706	0.00021
NM_005216.5(DDOST):c.999C>T (p.Gly333=)	rs190780604	0.00017
NM_005216.5(DDOST):c.154+19G>C	rs200373074	0.00004
NC_000001.11:g.20661380G>C	rs537816
NM_005216.5(DDOST):c.1063+34dup	rs11428148

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