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 212210027 rs17018378 G A rs17018378 4.92E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 1 212237798 rs10863936 G A rs10863936 2.00E-09 Height HPOID:0000002 NA A intron GWASdb_trait 1 212262467 rs10863938 T C rs10863938 2.68E-04 Stroke HPOID:0001297 DOID:6713 C intron GWASdb_trait 1 212266531 rs1586660 C G rs1586660 1.80E-06 Urinary metabolites HPOID:0000079 DOID:557 C intron GWASdb_trait 1 212273639 rs3135474 C T rs3135474 2.41E-04 Stroke HPOID:0001297 DOID:6713 T missense 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 rs1387815 1 212277107 212277107 UTR3 0.429687 0.36684778551477 GWAS of prostate cancer rs3738449 1 212240063 212240063 intronic 0.043109 1.36543205136367 GWAS of prostate cancer rs3135474 1 212273639 212273639 exonic 0.033477 1.47525346769855 GWAS of prostate cancer rs10863938 1 212262467 212262467 intronic 0.028649 1.5428905325818099 GWAS of prostate cancer rs7545292 1 212279058 212279058 downstream 0.000382 3.4179366370882898

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000143476.17 DTL 610617