Disease associated variation - GWASdb Chr Pos SNP ID(dbSNP 142) Ref Alt Ori SNP ID P-value Drug Name Drug Anno GWAS Trait HPO ID DO ID AA Type Trait or Drug 17 73256533 rs8073890 T C rs8073890 9.61E-05 WARFARIN VITAMIN K EPOXIDE REDUCTASES|CYTOCHROME P-450 CYP2C9|CYP4F2 PROTEIN, HUMAN|MIXED FUNCTION OXYGENASES|VKORC1 PROTEIN, HUMAN|CYP2C9 PROTEIN, HUMAN|CYTOCHROME P-450 ENZYME SYSTEM|ARYL HYDROCARBON HYDROXYLASES Warfarin maintenance dose HPOID:0004360 DOID:3393|DOID:9477 T intron GWASdb_drug 17 73256347 rs3760203 C G rs3760203 1.03E-04 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait 17 73256445 rs10512603 A G rs10512603 1.03E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 17 73256533 rs8073890 T C rs8073890 9.61E-05 Warfarin maintenance dose HPOID:0004360 DOID:3393|DOID:9477 T intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000125447.16 GGA3 606006