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 19 4360543 rs7769 G A rs7769 9.68E-12 Red blood cell traits HPOID:0001877 DOID:74 G UTR-3 GWASdb_trait 19 4365397 rs107288 T C rs107288 5.69E-09 Red blood cell traits HPOID:0001877 DOID:74 C intron GWASdb_trait 19 4366219 rs732716 A G rs732716 5.98E-13 Red blood cell traits HPOID:0001877 DOID:74 A intron GWASdb_trait 19 4375162 rs11085073 G A rs11085073 4.90E-12 Red blood cell traits HPOID:0001877 DOID:74 G intron GWASdb_trait 19 4386352 rs11085074 A G rs11085074 1.68E-10 Red blood cell traits HPOID:0001877 DOID:74 G intron GWASdb_trait 19 4391485 rs2247205 C T rs2247205 7.91E-09 Red blood cell traits HPOID:0001877 DOID:74 G intron GWASdb_trait 19 4394310 rs73234 G C rs73234 1.30E-09 Red blood cell traits HPOID:0001877 DOID:74 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000141985.9 SH3GL1 601768