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 10713932 rs4668690 G A rs4668690 5.12E-04 Type 2 diabetes HPOID:0005978 DOID:9352 G intron GWASdb_trait 2 10713932 rs4668690 G A rs4668690 8.05E-05 Systemic sclerosis HPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0000362|HPOID:0006918|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634 DOID:418 G intron GWASdb_trait 2 10737673 rs10490187 G A rs10490187 6.80E-04 Rheumatoid Arthritis (Cyclic citrullinated peptide positive) HPOID:0001370 DOID:7148 G intron GWASdb_trait 2 10761985 rs12476937 C T rs12476937 3.53E-05 Intracerebral hemorrhage HPOID:0001342 DOID:6713 T 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 rs1012580 2 10807748 10807748 intronic 0.763362 0.117269462936918 GWAS of prostate cancer rs2287059 2 10717806 10717806 exonic 0.708897 0.14941686154640602

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000115761.15 NOL10 616197