CN078013[trait identifier] AND "Medical Genetics Summaries"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 39381	CYP2D6*41	CYP2D6	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign; drug response; other
Select item 16889	CYP2D6*4	CYP2D6	Single nucleotide variant (splice acceptor variant)	not specified +3 more	GLikely benign; drug response; 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 830235	CYP2D6*17	CYP2D6 (T107I +4 more)	Single nucleotide variant (missense variant)	Tamoxifen response +1 more	Gdrug response
Select item 16893	CYP2D6*10	CYP2D6 (P34S)	Single nucleotide variant (missense variant)	not provided +3 more	GLikely benign; drug response; other
Select item 16890	CYP2D6*5	CYP2D6	Deletion	Tamoxifen response	Gdrug response

ClinVar