"Eurofins Ntd Llc (ga)"[submitter] AND "DRD2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 198436	NM_000795.4(DRD2):c.957C>T (p.Pro319=)	DRD2	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 256813	NM_000795.4(DRD2):c.932C>G (p.Ser311Cys)	DRD2 (S311C +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 256812	NM_000795.4(DRD2):c.928C>T (p.Pro310Ser)	DRD2 (P310S +1 more)	Single nucleotide variant (missense variant)	Dystonic disorder +3 more	GConflicting classifications of pathogenicity
Select item 198103	NM_000795.4(DRD2):c.731G>C (p.Cys244Ser)	DRD2 (C244S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 287221	NM_000795.4(DRD2):c.667G>A (p.Val223Ile)	DRD2 (V223I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 284673	NM_000795.4(DRD2):c.432G>A (p.Thr144=)	DRD2	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance

ClinVar