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 10 35303334 rs7920095 G A rs7920095 2.20E-05 Parkinson's disease HPOID:0001300 DOID:14330 A intron GWASdb_trait 10 35309367 rs7923172 G A rs7923172 1.43E-05 Parkinson's disease HPOID:0001300 DOID:14330 A intron GWASdb_trait 10 35326263 rs11595898 T C rs11595898 2.31E-05 Parkinson's disease HPOID:0001300 DOID:14330 T intron GWASdb_trait 10 35328088 rs11010077 A G rs11010077 8.06E-05 Multiple complex diseases HPOID:0000118 NA G,A intron GWASdb_trait 10 35332164 rs4934704 C T rs4934704 1.48E-05 Parkinson's disease HPOID:0001300 DOID:14330 T intron GWASdb_trait 10 35338673 rs7897024 C T rs7897024 6.21E-04 Multiple complex diseases HPOID:0000118 NA C cds-synon GWASdb_trait 10 35338699 rs7900480 G A rs7900480 1.10E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 10 35339324 rs4934709 C A rs4934709 9.19E-05 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait 10 35344969 rs1926554 C T rs1926554 3.32E-05 Parkinson's disease HPOID:0001300 DOID:14330 A intron GWASdb_trait 10 35349574 rs7099036 C T rs7099036 2.13E-05 Parkinson's disease HPOID:0001300 DOID:14330 T intron GWASdb_trait 10 35370465 rs13377158 G T rs13377158 1.82E-04 Multiple complex diseases HPOID:0000118 NA T intron GWASdb_trait 10 35376769 rs4934719 T C rs4934719 2.68E-05 Parkinson's disease HPOID:0001300 DOID:14330 C intron GWASdb_trait 10 35377715 rs4934721 A G rs4934721 1.39E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000108094.14 CUL2 603135