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 76811803 rs7218605 C T rs7218605 4.42E-06 Parkinson's disease HPOID:0001300 DOID:14330 T intron GWASdb_trait 17 76817090 rs3744793 C T rs3744793 7.24E-04 Type 2 diabetes HPOID:0005978 DOID:9352 G missense GWASdb_trait 17 76823227 rs3744792 T G rs3744792 6.58E-04 Type 2 diabetes HPOID:0005978 DOID:9352 A intron GWASdb_trait 17 76831800 rs7213204 T C rs7213204 9.87E-04 HIV-1 viral setpoint HPOID:0002721 DOID:526 C intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000055483.19 USP36 612543