"GeneDx"[submitter] AND "CYP2C9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58776	GRCh38/hg38 10q23.33-24.2(chr10:92626680-97755102)x1	LOC105378448, LOC107195252 +245 more	Copy number loss	See cases	GPathogenic
Select item 58777	GRCh38/hg38 10q23.33-24.32(chr10:93181201-101356779)x1	LOC130004555, LOC130004556 +375 more	Copy number loss	See cases	GPathogenic
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 773002	NM_000771.4(CYP2C9):c.752A>G (p.His251Arg)	CYP2C9 (H251R)	Single nucleotide variant (missense variant)	not provided	GBenign
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 225984	CYP2C9*5	CYP2C9 (D360E)	Single nucleotide variant (missense variant)	Flurbiprofen response +3 more	GBenign/Likely benign; drug response; other

ClinVar