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 6 43153409 rs16896326 G A rs16896326 7.16E-05 Schizophrenia HPOID:0100753 DOID:5419 G intron GWASdb_trait 6 43153787 rs61743561 G A rs61743561 9.00E-06 Obesity-related traits HPOID:0001513 DOID:9970 G missense GWASdb_trait 6 43168117 rs9462875 A G rs9462875 1.20E-21 Progranulin levels HPOID:0011018 DOID:9255 G intron GWASdb_trait 6 43168117 rs9462875 A G rs9462875 1.20E-21 Myocardial infarction HPOID:0001658 DOID:5844 G intron GWASdb_trait 6 43168117 rs9462875 A G rs9462875 1.46E-06 Schizophrenia HPOID:0100753 DOID:5419 G intron GWASdb_trait 6 43168117 rs9462875 A G rs9462875 0.000161 Schizophrenia HPOID:0100753 DOID:5419 G intron GWASdb_trait 6 43184132 rs2273709 A C rs2273709 2.60E-06 Schizophrenia HPOID:0100753 DOID:5419 C missense GWASdb_trait 6 43184132 rs2273709 A C rs2273709 0.0000082 Psychosis HPOID:0000709 DOID:2468 C missense GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000112659.13 CUL9 607489