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 9 77708152 rs3780178 T C rs3780178 5.70E-06 Urinary metabolites HPOID:0000079 DOID:557 T intron GWASdb_trait 9 77708152 rs3780178 T C rs3780178 2.92E-06 Lymphocyte counts HPOID:0004332|HPOID:0002665 DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287 T intron GWASdb_trait 9 77710789 rs1977240 T C rs1977240 9.10E-05 Type 2 diabetes HPOID:0005978 DOID:9352 C intron GWASdb_trait 9 77713279 rs10123421 A G rs10123421 1.36E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 9 77713279 rs10123421 A G rs10123421 3.02E-04 Coronary Artery Disease HPOID:0001677 DOID:3393 G intron GWASdb_trait 9 77719556 rs10869501 C G rs10869501 8.25E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 9 77754734 rs10869510 A T rs10869510 2.40E-05 Urinary metabolites HPOID:0000079 DOID:557 A intron GWASdb_trait 9 77755469 rs2273770 C T rs2273770 4.77E-05 Cognitive performance HPOID:0100543 DOID:1561 C intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000134996.11 OSTF1 610180