| 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 | 73885805 | rs1551619 | C | T | rs1551619 | 2.00E-07 | | | White matter hyperintensity burden | HPOID:0007103|HPOID:0002637 | DOID:936|DOID:2316|DOID:3527 | C | UTR-3 | GWASdb_trait |
| 17 | 73885805 | rs1551619 | C | T | rs1551619 | 0.000000553 | | | white matter hyperintensity burden | HPOID:0007103|HPOID:0002637 | DOID:936|DOID:2316|DOID:3527 | C | UTR-3 | GWASdb_trait |
| 17 | 73886888 | rs3760128 | A | G | rs3760128 | 8.00E-07 | | | White matter hyperintensity burden | HPOID:0007103|HPOID:0002637 | DOID:936|DOID:2316|DOID:3527 | G | missense | GWASdb_trait |
| 17 | 73886888 | rs3760128 | A | G | rs3760128 | 0.00000313 | | | white matter hyperintensity burden | HPOID:0007103|HPOID:0002637 | DOID:936|DOID:2316|DOID:3527 | G | missense | GWASdb_trait |
| 17 | 73888672 | rs3744028 | T | C | rs3744028 | 4.00E-15 | | | White matter hyperintensity burden | HPOID:0007103|HPOID:0002637 | DOID:936|DOID:2316|DOID:3527 | A | intron | GWASdb_trait |
| 17 | 73888672 | rs3744028 | T | C | rs3744028 | 6.39E-09 | | | white matter hyperintensity burden | HPOID:0007103|HPOID:0002637 | DOID:936|DOID:2316|DOID:3527 | A | intron | GWASdb_trait |