ClinVar for MedGen (Select 332377) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 16894	NM_000106.6(CYP2D6):c.775del (p.Arg259fs)	CYP2D6 (R259fs +1 more)	Deletion (frameshift variant)	not provided	GLikely benign; other
Select item 16893	CYP2D6*10	CYP2D6 (P34S)	Single nucleotide variant (missense variant)	not specified +3 more	GLikely benign; drug response; other
Select item 16892	NM_000106.5(CYP2D6):c.505G>T (p.Gly169Ter)	CYP2D6 (G169*)	Single nucleotide variant (nonsense +1 more)	not provided	GLikely benign; other
Select item 16891	CYP2D6*6	CYP2D6 (W152fs)	Deletion (frameshift variant +1 more)	not provided +2 more	GBenign/Likely benign; drug response; other
Select item 16890	CYP2D6*5	CYP2D6	Deletion	Tamoxifen response	Gdrug response
Select item 16889	CYP2D6*4	CYP2D6	Single nucleotide variant (splice acceptor variant)	Deutetrabenazine response +3 more	GLikely benign; drug response; other

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