"PreventionGenetics, part of Exact Sciences"[submitter] AND "MGAT2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 313254	NM_002408.4(MGAT2):c.63C>T (p.Gly21=)	MGAT2	Single nucleotide variant (synonymous variant)	MGAT2-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 3031582	NM_002408.4(MGAT2):c.69C>T (p.Val23=)	MGAT2	Single nucleotide variant (synonymous variant)	MGAT2-related disorder	GLikely benign
Select item 218607	NM_002408.4(MGAT2):c.99G>T (p.Lys33Asn)	MGAT2 (K33N)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 2083378	NM_002408.4(MGAT2):c.216G>A (p.Ala72=)	MGAT2	Single nucleotide variant (synonymous variant)	MGAT2-related disorder +1 more	GBenign/Likely benign
Select item 702828	NM_002408.4(MGAT2):c.229C>T (p.Pro77Ser)	MGAT2 (P77S)	Single nucleotide variant (missense variant)	MGAT2-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 736435	NM_002408.4(MGAT2):c.636T>C (p.Asn212=)	MGAT2	Single nucleotide variant (synonymous variant)	MGAT2-related disorder +1 more	GLikely benign
Select item 163091	NM_018139.3(DNAAF2):c.2303A>G (p.Asp768Gly)	DNAAF2, MGAT2 (D768G +2 more)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign

ClinVar