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 1 150790762 rs7518440 A G rs7518440 0.000000172 Cholesterol, total HPOID:0003107 DOID:3393|DOID:3146|DOID:2349 G intron GWASdb_trait 1 150790762 rs7518440 A G rs7518440 4.06E-08 HDL cholesterol HPOID:0003107 DOID:14502|DOID:1461|DOID:3393 G intron GWASdb_trait 1 150811005 rs10305685 T C rs10305685 3.47E-08 HDL cholesterol HPOID:0003107 DOID:14502|DOID:1461|DOID:3393 A intron GWASdb_trait 1 150848977 rs10305650 G A rs10305650 2.01E-08 HDL cholesterol HPOID:0003107 DOID:14502|DOID:1461|DOID:3393 C intron GWASdb_trait

Disease associated variation - GWAS Central Study Name Source Marker Accession Chromosome Marker Start Marker Stop Alleles Gene Section P-value -log(p-value) GWAS of prostate cancer rs2134688 1 150816886 150816886 intronic 0.57721 0.23866615348429798 GWAS of prostate cancer rs10305724 1 150795365 150795365 intronic 0.555117 0.255615472554391

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000143437.20 ARNT 126110