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 | 47661493 | rs307896 | G | A | rs307896 | 5.00E-07 | | | Multiple sclerosis | HPOID:0000096|HPOID:0001967|HPOID:0009741|HPOID:0008664|HPOID:0001150|HPOID:0005450|HPOID:0005652|HPOID:0005686|HPOID:0005789|HPOID:0100923|HPOID:0100925|HPOID:0006623|HPOID:0100861|HPOID:0002694|HPOID:0004979|HPOID:0003881|HPOID:0003991|HPOID:0003854|HPOID:0003933|HPOID:0004030|HPOID:0100899|HPOID:0002634 | DOID:2377 | C | intron | GWASdb_trait | 19 | 47664951 | rs17729227 | T | C | rs17729227 | 1.14E-04 | | | Multiple complex diseases | HPOID:0000118 | NA | T | intron | GWASdb_trait | 19 | 47689921 | rs3745621 | C | G | rs3745621 | 3.10E-04 | | | Height | HPOID:0000002 | NA | G | intron | GWASdb_trait | |