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 19 3005231 rs216279 G C rs216279 2.31E-05 Type 2 diabetes HPOID:0005978 DOID:9352 G intron GWASdb_trait 19 3006274 rs83488 C T rs83488 9.26E-04 Amyotrophic Lateral Sclerosis HPOID:0007354 DOID:332 A intron GWASdb_trait 19 3013374 rs3760961 A G rs3760961 8.68E-05 ldl cholesterol HPOID:0010979 DOID:1936|DOID:3393 A intron GWASdb_trait 19 3013374 rs3760961 A G rs3760961 4.17E-06 Cholesterol HPOID:0003107 DOID:2349|DOID:3393|DOID:3146 A intron GWASdb_trait 19 3020691 rs7249809 A G rs7249809 3.10E-06 Lung adenocarcinoma HPOID:0100526 DOID:3910 G intron GWASdb_trait 19 3030168 rs1688128 T C rs1688128 8.27E-04 Parkinson's disease HPOID:0001300 DOID:14330 A intron GWASdb_trait 19 3030168 rs1688128 T C rs1688128 6.60E-05 Lung adenocarcinoma HPOID:0100526 DOID:3910 A intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000065717.14 TLE2 601041