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 46929873 rs11676737 T C rs11676737 3.06E-04 Hemoglobin concentration HPOID:0011902 DOID:2860 T intron GWASdb_trait 2 46938789 rs13025984 T C rs13025984 3.06E-04 Hemoglobin concentration HPOID:0011902 DOID:2860 T intron GWASdb_trait 2 46957845 rs4952843 A G rs4952843 3.06E-04 Hemoglobin concentration HPOID:0011902 DOID:2860 A intron GWASdb_trait 2 46978349 rs11695058 A G rs11695058 9.96E-07 Lymphocyte counts HPOID:0004332|HPOID:0002665 DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287 A intron GWASdb_trait 2 46988073 rs17823065 T C rs17823065 6.49E-04 Multiple complex diseases HPOID:0000118 NA T UTR-3 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 rs6741642 2 46934908 46934908 intronic 0.975093 0.010953961264872 GWAS of prostate cancer rs4953418 2 46984627 46984627 intronic 0.842341 0.0745120599989457 GWAS of prostate cancer rs973491 2 46930776 46930776 intronic 0.809186 0.0919516397115931 GWAS of prostate cancer rs10167561 2 46968051 46968051 intronic 0.644025 0.19109727370957902

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000171150.7 SOCS5 607094