"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "DGAT2"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 708403	NM_032564.5(DGAT2):c.690T>C (p.Ser230=)	DGAT2	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2642161	NM_032564.5(DGAT2):c.749G>A (p.Gly250Asp)	DGAT2 (G207D +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2642162	NM_032564.5(DGAT2):c.855C>A (p.Tyr285Ter)	DGAT2 (Y242* +1 more)	Single nucleotide variant (nonsense)	not provided	GBenign
Select item 2642163	NM_032564.5(DGAT2):c.889C>T (p.Arg297Ter)	DGAT2 (R254* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1284806	NM_032564.5(DGAT2):c.890G>A (p.Arg297Gln)	DGAT2 (R254Q +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2642164	NM_032564.5(DGAT2):c.952G>A (p.Gly318Ser)	DGAT2 (G275S +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar