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 182664547 rs4859259 G A rs4859259 1.96E-04 IgE levels HPOID:0010701 DOID:6024 G intron GWASdb_trait 3 182669780 rs6786608 G A rs6786608 7.46E-04 Acute lung injury HPOID:0002088 DOID:850 G intron GWASdb_trait 3 182670993 rs10937104 A T rs10937104 3.72E-04 Acute lung injury HPOID:0002088 DOID:850 A intron GWASdb_trait 3 182671158 rs9814216 C T rs9814216 1.07E-06 Parkinson's disease HPOID:0001300 DOID:14330 T,C intron GWASdb_trait 3 182673196 rs7641401 C T rs7641401 7.18E-04 Type 2 diabetes HPOID:0005978 DOID:9352 T intron GWASdb_trait 3 182681074 rs13093344 G C rs13093344 7.19E-04 Acute lung injury HPOID:0002088 DOID:850 G intron GWASdb_trait 3 182681853 rs4859147 T C rs4859147 3.54E-04 Acute lung injury HPOID:0002088 DOID:850 T intron GWASdb_trait 3 182685440 rs4859148 G A rs4859148 2.85E-05 Parkinson's disease HPOID:0001300 DOID:14330 A intron GWASdb_trait 3 182685440 rs4859148 G A rs4859148 6.41E-04 Acute lung injury HPOID:0002088 DOID:850 A intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000043093.13 DCUN1D1 605905