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 20924077 rs7226229 C T rs7226229 1.00E-06 ZINC SELENIUM|COPPER Blood trace element (Se levels) HPOID:0001877 DOID:74 C intron GWASdb_drug 17 20904451 rs1044414 A G rs1044414 6.88E-04 Heart Failure HPOID:0001635 DOID:6000 T UTR-3 GWASdb_trait 17 20910424 rs9914758 T C rs9914758 7.27E-04 Body mass index HPOID:0001507 DOID:9970 T intron GWASdb_trait 17 20914156 rs9909279 G A rs9909279 4.74E-04 Body mass index HPOID:0001507 DOID:9970 G intron GWASdb_trait 17 20924077 rs7226229 C T rs7226229 1.00E-06 Blood trace element (Se levels) HPOID:0001877 DOID:74 C intron GWASdb_trait 17 20934127 rs2127096 C T rs2127096 2.28E-04 Body mass index HPOID:0001507 DOID:9970 C,T intron GWASdb_trait 17 20938791 rs1993901 A G rs1993901 6.04E-04 Heart Failure HPOID:0001635 DOID:6000 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000124422.11 USP22 612116