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 10 62634621 rs2279942 C T rs2279942 5.54E-04 Fibrinogen HPOID:0011898 DOID:1287 A intron GWASdb_trait 10 62640118 rs10821850 C G rs10821850 2.53E-04 Fibrinogen HPOID:0011898 DOID:1287 G intron GWASdb_trait 10 62650130 rs16915679 G A rs16915679 9.26E-05 Height HPOID:0000002 NA G intron GWASdb_trait 10 62652165 rs7898435 T C rs7898435 8.76E-05 Non-alcoholic fatty liver disease histology (other) HPOID:0001397|HPOID:0006561 DOID:9452 T intron GWASdb_trait 10 62662314 rs750593 A G rs750593 2.00E-05 Urinary metabolites HPOID:0000079 DOID:557 C intron GWASdb_trait 10 62662503 rs4437981 T C rs4437981 2.00E-05 Urinary metabolites HPOID:0000079 DOID:557 C intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000072422.16 RHOBTB1 607351