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 12 109909011 rs2058804 A G rs2058804 2.40E-05 CHOLESTEROL LIPOPROTEINS|TRIGLYCERIDES Lipid levels HPOID:0003119 DOID:3146|DOID:1287|DOID:9970 C intron GWASdb_drug 12 109909011 rs2058804 A G rs2058804 5.50E-05 CHOLESTEROL LIPOPROTEINS|TRIGLYCERIDES Lipid levels HPOID:0003119 DOID:3146|DOID:1287|DOID:9970 C intron GWASdb_drug 12 109909011 rs2058804 A G rs2058804 5.80E-06 CHOLESTEROL LIPOPROTEINS|TRIGLYCERIDES Lipid levels HPOID:0003119 DOID:3146|DOID:1287|DOID:9970 C intron GWASdb_drug 12 109888779 rs1477117 G A rs1477117 3.23E-04 Scoliosis HPOID:0010674 DOID:0080010 C UTR-3 GWASdb_trait 12 109888779 rs1477117 G A rs1477117 2.20E-05 Urinary metabolites HPOID:0000079 DOID:557 C UTR-3 GWASdb_trait 12 109888779 rs1477117 G A rs1477117 3.70E-04 Atrial fibrillation HPOID:0005110 DOID:0050650 C UTR-3 GWASdb_trait 12 109890080 rs4766601 G C rs4766601 9.83E-04 Type 2 diabetes HPOID:0005978 DOID:9352 G intron GWASdb_trait 12 109890080 rs4766601 G C rs4766601 5.51E-26 Lymphocyte counts HPOID:0004332|HPOID:0002665 DOID:2841|DOID:1240|DOID:0060058|DOID:614|DOID:1287 G intron GWASdb_trait 12 109890339 rs9943689 G A rs9943689 5.87E-05 Body Composition HPOID:0001513|HPOID:0001627 DOID:9970|DOID:114 A intron GWASdb_trait 12 109893156 rs10774708 A G rs10774708 9.20E-08 Lipid levels HPOID:0003119 DOID:3146|DOID:1287|DOID:9970 G intron GWASdb_trait 12 109895168 rs2338104 C G rs2338104 3.00E-08 HDL cholesterol HPOID:0003107 DOID:14502|DOID:1461|DOID:3393 G intron GWASdb_trait 12 109895168 rs2338104 C G rs2338104 1.00E-10 HDL cholesterol HPOID:0003107 DOID:14502|DOID:1461|DOID:3393 G intron GWASdb_trait 12 109895168 rs2338104 C G rs2338104 1.00E-10 Coronary heart disease HPOID:0001677 DOID:3393 G intron GWASdb_trait 12 109903062 rs10850201 C G rs10850201 4.88E-04 Body mass index HPOID:0001507 DOID:9970 C intron GWASdb_trait 12 109904198 rs918107 T C rs918107 1.00E-05 Urinary metabolites HPOID:0000079 DOID:557 A intron GWASdb_trait 12 109904792 rs11066737 G A rs11066737 4.49E-04 Type 2 diabetes HPOID:0005978 DOID:9352 A intron GWASdb_trait 12 109904792 rs11066737 G A rs11066737 1.00E-05 Urinary metabolites HPOID:0000079 DOID:557 A intron GWASdb_trait 12 109909011 rs2058804 A G rs2058804 2.40E-05 Lipid levels HPOID:0003119 DOID:3146|DOID:1287|DOID:9970 C intron GWASdb_trait 12 109909011 rs2058804 A G rs2058804 5.50E-05 Lipid levels HPOID:0003119 DOID:3146|DOID:1287|DOID:9970 C intron GWASdb_trait 12 109909011 rs2058804 A G rs2058804 5.80E-06 Lipid levels HPOID:0003119 DOID:3146|DOID:1287|DOID:9970 C intron GWASdb_trait 12 109909011 rs2058804 A G rs2058804 4.07E-04 Alzheimer's disease (late onset) HPOID:0002511 DOID:10652 C intron GWASdb_trait 12 109909011 rs2058804 A G rs2058804 6.08E-05 Neuroblastoma HPOID:0003006 DOID:769 C intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000110906.12 KCTD10 613421