ClinVar for MedGen (Select 322023) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 163021	NM_000771.3(CYP2C9):c.[430C=;1075A>C]	CYP2C9 (I359L)	Single nucleotide variant (missense variant +1 more)	Warfarin response	Gdrug response
Select item 8408	CYP2C9*3	CYP2C9 (I359L)	Single nucleotide variant (missense variant)	not provided +3 more	Gdrug response; other