List of variants in gene COG6 reported as uncertain significance for Congenital disorder of glycosylation

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_020751.3(COG6):c.-21_-20insC	rs746938820	0.00041
NM_020751.3(COG6):c.*1443A>T	rs772109615	0.00014
NM_020751.3(COG6):c.*205C>G	rs886050232	0.00001
NM_020751.2(COG6):c.-67A>T	rs548475910
NM_020751.3(COG6):c.*1438AGA[1]	rs886050235
NM_020751.3(COG6):c.*147dup	rs554269460

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