| 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 |
|---|
| 3 | 49322027 | rs2304442 | T | A | rs2304442 | 5.07E-05 | | | Multiple complex diseases | HPOID:0000118 | NA | T | intron | GWASdb_trait | | 3 | 49326178 | rs9874474 | A | G | rs9874474 | 1.31E-06 | | | Crohn's disease | HPOID:0100280 | DOID:8778 | G | intron | GWASdb_trait | | 3 | 49329090 | rs4410472 | A | T | rs4410472 | 1.75E-05 | | | Multiple complex diseases | HPOID:0000118 | NA | T | intron | GWASdb_trait | | 3 | 49329090 | rs4410472 | A | T | rs4410472 | 1.53E-06 | | | Crohn's disease | HPOID:0100280 | DOID:8778 | T | intron | GWASdb_trait | | 3 | 49343175 | rs2230929 | G | A,C,T | rs2230929 | 1.38E-06 | | | Crohn's disease | HPOID:0100280 | DOID:8778 | C | missense | GWASdb_trait | | 3 | 49352619 | rs9864406 | T | C | rs9864406 | 4.57E-05 | | | Multiple complex diseases | HPOID:0000118 | NA | C | intron | GWASdb_trait | | 3 | 49359943 | rs9873994 | T | C | rs9873994 | 1.63E-06 | | | Crohn's disease | HPOID:0100280 | DOID:8778 | T | intron | GWASdb_trait | | 3 | 49366741 | rs9863142 | G | C | rs9863142 | 6.89E-05 | | | Multiple complex diseases | HPOID:0000118 | NA | C | intron | GWASdb_trait | | 3 | 49366741 | rs9863142 | G | C | rs9863142 | 1.32E-06 | | | Crohn's disease | HPOID:0100280 | DOID:8778 | C | intron | GWASdb_trait | |