Related gene-specific medical variations for Gene (Select 1815) - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065404	NM_000797.4(DRD4):c.759_806dup (p.Pro270_Arg271insGlnAspProCysGlyProAspCysAlaProProAlaProGlyLeuPro)	DRD4	Duplication (inframe_insertion)	Hereditary attention deficit-hyperactivity disorder	GUncertain significance
Select item 3065214	NM_000797.4(DRD4):c.155dup (p.Asn52fs)	DRD4 (N52fs)	Duplication (frameshift variant)	Hereditary attention deficit-hyperactivity disorder	GLikely pathogenic
Select item 2688971	NM_000797.4(DRD4):c.793_840del (p.Pro265_Pro280del)	DRD4	Deletion (inframe_deletion)	not provided	GUncertain significance

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