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 17 76000573 rs8074332 T C rs8074332 4.16E-04 Alzheimer's disease HPOID:0002511 DOID:10652 C intron GWASdb_trait 17 76012854 rs4789523 C T rs4789523 6.95E-05 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait 17 76012854 rs4789523 C T rs4789523 1.66E-05 Alzheimer's disease HPOID:0002511 DOID:10652 C intron GWASdb_trait 17 76026671 rs9889827 T C rs9889827 8.74E-05 Alzheimer's disease HPOID:0002511 DOID:10652 T,C intron GWASdb_trait 17 76030028 rs16970755 G A rs16970755 2.33E-06 Personality dimensions HPOID:0012075 DOID:1510 G intron GWASdb_trait 17 76030028 rs16970755 G A rs16970755 1.77E-04 Alzheimer's disease HPOID:0002511 DOID:10652 G intron GWASdb_trait 17 76033562 rs4362447 C T rs4362447 6.46E-06 Multiple complex diseases HPOID:0000118 NA C intron GWASdb_trait 17 76033562 rs4362447 C T rs4362447 3.36E-04 Alzheimer's disease HPOID:0002511 DOID:10652 C intron GWASdb_trait 17 76039419 rs16970766 G C rs16970766 1.50E-04 Alzheimer's disease HPOID:0002511 DOID:10652 G intron GWASdb_trait 17 76054749 rs2311443 C G rs2311443 1.30E-04 Alzheimer's disease HPOID:0002511 DOID:10652 C intron GWASdb_trait 17 76055547 rs16970774 G A rs16970774 1.30E-04 Alzheimer's disease HPOID:0002511 DOID:10652 G intron GWASdb_trait 17 76056144 rs9916037 T C rs9916037 1.26E-04 Alzheimer's disease HPOID:0002511 DOID:10652 C intron GWASdb_trait 17 76057354 rs2311442 A G rs2311442 1.28E-04 Alzheimer's disease HPOID:0002511 DOID:10652 T intron GWASdb_trait 17 76057435 rs2871765 A C rs2871765 1.29E-04 Alzheimer's disease HPOID:0002511 DOID:10652 T intron GWASdb_trait 17 76058682 rs16970784 A T rs16970784 2.16E-04 Multiple complex diseases HPOID:0000118 NA T intron GWASdb_trait 17 76059782 rs9893684 A G rs9893684 1.43E-04 Alzheimer's disease HPOID:0002511 DOID:10652 G intron GWASdb_trait 17 76061566 rs4789012 C A rs4789012 5.87E-05 Multiple complex diseases HPOID:0000118 NA A intron GWASdb_trait 17 76061566 rs4789012 C A rs4789012 3.15E-04 Alzheimer's disease HPOID:0002511 DOID:10652 A intron GWASdb_trait 17 76077700 rs9909805 A G rs9909805 1.07E-04 Alzheimer's disease HPOID:0002511 DOID:10652 G intron GWASdb_trait 17 76092553 rs2311001 G C rs2311001 1.05E-04 Alzheimer's disease HPOID:0002511 DOID:10652 G intron GWASdb_trait 17 76092553 rs2311001 G C rs2311001 3.14E-04 Schizophrenia HPOID:0100753 DOID:5419 G intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000078687.17 TNRC6C 610741