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 73871467 rs3744017 G A rs3744017 7.30E-09 White matter hyperintensity burden HPOID:0007103|HPOID:0002637 DOID:936|DOID:2316|DOID:3527 G intron GWASdb_trait 17 73871467 rs3744017 G A rs3744017 8.49E-09 white matter hyperintensity burden HPOID:0007103|HPOID:0002637 DOID:936|DOID:2316|DOID:3527 G intron GWASdb_trait 17 73872948 rs1055129 A G rs1055129 3.00E-11 White matter hyperintensity burden HPOID:0007103|HPOID:0002637 DOID:936|DOID:2316|DOID:3527 C intron GWASdb_trait 17 73872948 rs1055129 A G rs1055129 3.58E-08 white matter hyperintensity burden HPOID:0007103|HPOID:0002637 DOID:936|DOID:2316|DOID:3527 C intron GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000132481.6 TRIM47 611041