CN258188[trait identifier] AND "Medical Genetics Summaries"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 8409	CYP2C9*2	CYP2C9 (R144C)	Single nucleotide variant (missense variant)	not specified +4 more	GLikely benign; drug response; other
Select item 226024	CYP2C9*8	CYP2C9 (R150H)	Single nucleotide variant (missense variant)	Piroxicam response +3 more	GBenign/Likely benign; drug response
Select item 285601	CYP2C9*6	CYP2C9 (K273fs)	Deletion (frameshift variant)	Flurbiprofen response +3 more	GBenign/Likely benign; drug response; other
Select item 370010	CYP2C9*11	CYP2C9 (R335W)	Single nucleotide variant (missense variant)	Piroxicam response +3 more	GBenign/Likely benign; drug response
Select item 8408	CYP2C9*3	CYP2C9 (I359L)	Single nucleotide variant (missense variant)	Flurbiprofen response +3 more	Gdrug response; other
Select item 225984	CYP2C9*5	CYP2C9 (D360E)	Single nucleotide variant (missense variant)	Flurbiprofen response +3 more	GBenign/Likely benign; drug response; other

ClinVar