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 7 27780476 rs11520772 A T rs11520772 2.86E-04 Bone properties (heel) HPOID:0000939 DOID:11476 A intron GWASdb_trait 7 27787009 rs4722740 T C rs4722740 0.00023 Coronary artery calcification HPOID:0001677 DOID:3393 T intron GWASdb_trait 7 27796710 rs17155787 G A rs17155787 1.88E-04 Multiple complex diseases HPOID:0000118 NA G intron GWASdb_trait 7 27833693 rs1544414 T G rs1544414 2.15E-08 Lymphocyte counts HPOID:0004332|HPOID:0002665 DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287 T intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000106052.13 TAX1BP1 605326