"PreventionGenetics, part of Exact Sciences"[submitter] AND "OGT"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3061687	NM_181672.3(OGT):c.522A>C (p.Glu174Asp)	OGT (E164D +1 more)	Single nucleotide variant (missense variant)	OGT-related disorder	GUncertain significance
Select item 720641	NM_181672.3(OGT):c.1281A>C (p.Ala427=)	OGT	Single nucleotide variant (synonymous variant)	OGT-related disorder +1 more	GBenign
Select item 3040554	NM_181672.3(OGT):c.1536A>G (p.Leu512=)	OGT	Single nucleotide variant (synonymous variant)	OGT-related disorder	GLikely benign
Select item 2632277	NM_181672.3(OGT):c.1663C>T (p.Arg555Trp)	OGT (R545W +1 more)	Single nucleotide variant (missense variant)	OGT-related disorder	GUncertain significance
Select item 1601086	NM_181672.3(OGT):c.2652T>G (p.Pro884=)	OGT	Single nucleotide variant (synonymous variant)	OGT-related disorder +1 more	GBenign/Likely benign
Select item 2059816	NM_181672.3(OGT):c.2841A>G (p.Pro947=)	OGT	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign

ClinVar