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 17 73315368 rs7219 C T rs7219 0.00007295 Sarcoidosis HPOID:0012220 DOID:11335 A UTR-3 GWASdb_trait 17 73317644 rs12946365 C T rs12946365 4.57E-06 Systemic lupus erythematosus and Systemic sclerosis HPOID:0002725 DOID:9074|DOID:1578 T intron GWASdb_trait 17 73320433 rs12938183 G C rs12938183 0.00007719 Sarcoidosis HPOID:0012220 DOID:11335 C intron GWASdb_trait 17 73325244 rs2164244 C T rs2164244 0.00005819 Sarcoidosis HPOID:0012220 DOID:11335 T intron GWASdb_trait 17 73328374 rs12600908 G A rs12600908 1.32E-05 Aging (time to event) HPOID:0000118 NA G intron GWASdb_trait 17 73328989 rs16967789 G A rs16967789 2.44E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 17 73328989 rs16967789 G A rs16967789 7.48E-04 Response to taxane treatment (placlitaxel) HPOID:0100526 DOID:1324 G intron GWASdb_trait 17 73333871 rs1966663 T C rs1966663 0.00009433 Sarcoidosis HPOID:0012220 DOID:11335 G intron GWASdb_trait 17 73342702 rs12940188 T C rs12940188 0.00009931 Sarcoidosis HPOID:0012220 DOID:11335 C intron GWASdb_trait 17 73343344 rs11077787 G C rs11077787 3.45E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 17 73343927 rs9900586 A C rs9900586 4.31E-04 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 17 73344079 rs12950752 A G rs12950752 0.00005831 Sarcoidosis HPOID:0012220 DOID:11335 G intron GWASdb_trait 17 73344711 rs1076094 T C rs1076094 2.74E-04 Multiple complex diseases HPOID:0000118 NA T intron GWASdb_trait 17 73369422 rs959260 C T rs959260 2.10E-06 Height HPOID:0000002 NA A intron GWASdb_trait 17 73369422 rs959260 C T rs959260 2.70E-04 Height HPOID:0000002 NA A intron GWASdb_trait 17 73374945 rs4789182 G A rs4789182 8.75E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 17 73374945 rs4789182 G A rs4789182 8.50E-07 Systemic lupus erythematosus and Systemic sclerosis HPOID:0002725 DOID:9074|DOID:1578 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000177885.13 GRB2 108355