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 3 101045977 rs473702 A G rs473702 1.31E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 3 101058775 rs5009801 A G rs5009801 9.99E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 3 101058775 rs5009801 A G rs5009801 5.92E-05 Schizophrenia HPOID:0100753 DOID:5419 A intron GWASdb_trait 3 101059816 rs3846085 G A rs3846085 6.97E-04 Smoking quantity HPOID:0000707 DOID:0050742 A,G intron GWASdb_trait 3 101068620 rs2553419 C T rs2553419 5.92E-05 Schizophrenia HPOID:0100753 DOID:5419 G intron GWASdb_trait 3 101068873 rs2682386 C T rs2682386 1.73E-04 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait 3 101069852 rs9877228 G C rs9877228 8.87E-05 Schizophrenia HPOID:0100753 DOID:5419 G intron GWASdb_trait 3 101072258 rs9875156 A C rs9875156 4.92E-05 Schizophrenia HPOID:0100753 DOID:5419 A intron GWASdb_trait 3 101106527 rs2553427 A G rs2553427 2.50E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 3 101106527 rs2553427 A G rs2553427 4.35E-05 Parkinson's disease HPOID:0001300 DOID:14330 A intron GWASdb_trait 3 101109166 rs9857723 A T rs9857723 4.65E-05 Schizophrenia HPOID:0100753 DOID:5419 T intron GWASdb_trait 3 101113177 rs1520653 C T rs1520653 7.03E-05 Schizophrenia HPOID:0100753 DOID:5419 T intron GWASdb_trait 3 101114990 rs12497154 G A rs12497154 4.10E-05 Schizophrenia HPOID:0100753 DOID:5419 A intron GWASdb_trait 3 101121980 rs2317749 A G rs2317749 1.14E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 3 101122120 rs2317750 C A rs2317750 5.92E-05 Schizophrenia HPOID:0100753 DOID:5419 A intron GWASdb_trait 3 101136340 rs9822356 C T rs9822356 7.54E-05 Schizophrenia HPOID:0100753 DOID:5419 T intron GWASdb_trait 3 101136402 rs9859077 G C rs9859077 2.68E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 3 101155038 rs9814840 T C rs9814840 9.01E-04 White matter integrity HPOID:0002500 DOID:3312|DOID:936 T intron GWASdb_trait 3 101165959 rs10936631 A G rs10936631 9.07E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 3 101165959 rs10936631 A G rs10936631 2.49E-05 Schizophrenia HPOID:0100753 DOID:5419 A intron GWASdb_trait 3 101177644 rs12496159 A C rs12496159 4.85E-05 Schizophrenia HPOID:0100753 DOID:5419 A intron GWASdb_trait 3 101179057 rs2141180 T C rs2141180 1.82E-04 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait 3 101181028 rs6441608 G A rs6441608 5.58E-05 Parkinson's disease HPOID:0001300 DOID:14330 A intron GWASdb_trait 3 101181890 rs2317703 T C rs2317703 5.92E-05 Schizophrenia HPOID:0100753 DOID:5419 C intron GWASdb_trait 3 101211487 rs3846087 A G rs3846087 1.38E-04 Schizophrenia HPOID:0100753 DOID:5419 T intron GWASdb_trait 3 101212855 rs6791803 T C rs6791803 3.83E-05 Tourette syndrome HPOID:0000709 DOID:11119|DOID:10933|DOID:1094 T,C intron GWASdb_trait 3 101220400 rs3846092 C T rs3846092 1.66E-04 Tourette syndrome HPOID:0000709 DOID:11119|DOID:10933|DOID:1094 C intron GWASdb_trait 3 101230304 rs2317704 C G rs2317704 8.78E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 3 101230304 rs2317704 C G rs2317704 4.26E-05 Schizophrenia HPOID:0100753 DOID:5419 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000138468.15 SENP7 612846