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 60778932 rs2251393 G A rs2251393 1.20E-14 Progranulin levels HPOID:0011018 DOID:9255 C UTR-3 GWASdb_trait 17 60778932 rs2251393 G A rs2251393 1.20E-14 Myocardial infarction HPOID:0001658 DOID:5844 C UTR-3 GWASdb_trait 17 60778932 rs2251393 G A rs2251393 4.00E-07 Sudden cardiac arrest HPOID:0001645 DOID:3393 C UTR-3 GWASdb_trait 17 60789059 rs9889540 G C rs9889540 4.52E-05 Depression (quantitative trait) HPOID:0000716 DOID:1596 C intron GWASdb_trait 17 60789316 rs9890213 G C rs9890213 3.66E-04 Depression (quantitative trait) HPOID:0000716 DOID:1596 G intron GWASdb_trait 17 60789405 rs9891713 T C rs9891713 5.17E-04 Depression (quantitative trait) HPOID:0000716 DOID:1596 C intron GWASdb_trait 17 60791818 rs1024653 A C rs1024653 3.57E-04 Type 2 diabetes HPOID:0005978 DOID:9352 T intron GWASdb_trait 17 60802483 rs17683483 C A rs17683483 1.07E-05 Alzheimer's disease (late onset) HPOID:0002511 DOID:10652 C intron GWASdb_trait 17 60802483 rs17683483 C A rs17683483 5.69E-04 Alzheimer's disease HPOID:0002511 DOID:10652 C intron GWASdb_trait 17 60841251 rs17684593 C T rs17684593 7.27E-05 Hypertension HPOID:0000822 DOID:10763 C,T intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000173838.11 MARCH10 613337