"PreventionGenetics, part of Exact Sciences"[submitter] AND "COG2"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 718942	NM_007357.3(COG2):c.218A>G (p.Asn73Ser)	COG2 (N73S)	Single nucleotide variant (missense variant)	COG2-related disorder +1 more	GLikely benign
Select item 672165	NM_007357.3(COG2):c.264T>G (p.Leu88=)	COG2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 478370	NM_007357.3(COG2):c.1014T>C (p.Asp338=)	COG2	Single nucleotide variant (synonymous variant)	COG2-related disorder +2 more	GBenign/Likely benign
Select item 779620	NM_007357.3(COG2):c.1532C>G (p.Thr511Ser)	COG2 (T511S)	Single nucleotide variant (missense variant)	Congenital disorder of glycosylation, type IIq +1 more	GLikely benign
Select item 1556615	NM_007357.3(COG2):c.1740C>T (p.Phe580=)	COG2	Single nucleotide variant (synonymous variant)	Congenital disorder of glycosylation, type IIq +1 more	GLikely benign
Select item 712899	NM_007357.3(COG2):c.1755C>T (p.Ser585=)	COG2	Single nucleotide variant (synonymous variant)	Congenital disorder of glycosylation, type IIq +1 more	GLikely benign

ClinVar