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 2 128060068 rs4233583 C A rs4233583 3.77E-14 Protein C levels HPOID:0003256 DOID:3756 C UTR-3 GWASdb_trait 2 128062048 rs3088374 T C rs3088374 3.81E-10 Protein C levels HPOID:0003256 DOID:3756 T UTR-3 GWASdb_trait 2 128071003 rs6731176 C T rs6731176 1.78E-09 Protein C levels HPOID:0003256 DOID:3756 T intron GWASdb_trait 2 128076022 rs9636237 T C rs9636237 6.44E-13 Protein C levels HPOID:0003256 DOID:3756 T intron GWASdb_trait 2 128076607 rs4662720 T C rs4662720 3.17E-21 Protein C levels HPOID:0003256 DOID:3756 C intron GWASdb_trait 2 128079806 rs3732209 A G rs3732209 1.01E-21 Protein C levels HPOID:0003256 DOID:3756 T cds-synon GWASdb_trait 2 128081682 rs12622436 C A rs12622436 3.42E-14 Protein C levels HPOID:0003256 DOID:3756 C intron GWASdb_trait 2 128082232 rs6430937 C T rs6430937 3.19E-04 Type 2 diabetes HPOID:0005978 DOID:9352 T intron GWASdb_trait 2 128082232 rs6430937 C T rs6430937 0.00041 Coronary artery calcification HPOID:0001677 DOID:3393 T intron GWASdb_trait 2 128086354 rs12613413 C T rs12613413 0.00036 Coronary artery calcification HPOID:0001677 DOID:3393 T intron GWASdb_trait 2 128089540 rs6732279 G T rs6732279 3.30E-14 Protein C levels HPOID:0003256 DOID:3756 G intron GWASdb_trait 2 128090144 rs10496661 G T rs10496661 3.41E-21 Protein C levels HPOID:0003256 DOID:3756 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000169967.16 MAP3K2 609487