| 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 |
|---|
| 18 | 71788676 | rs9945428 | C | A | rs9945428 | 7.00E-09 | FACTOR VIII | TRANSCRIPTION FACTORS|HOMEODOMAIN PROTEINS|IRX3 PROTEIN, HUMAN | Venous thromboembolism (gene x gene interaction) | HPOID:0002204|HPOID:0002625 | DOID:866|DOID:9477 | A | intron | GWASdb_drug |
| 18 | 71788676 | rs9945428 | C | A | rs9945428 | 7.00E-09 | | | Venous thromboembolism (gene x gene interaction) | HPOID:0002204|HPOID:0002625 | DOID:866|DOID:9477 | A | intron | GWASdb_trait |
| 18 | 71797093 | rs17088802 | G | C | rs17088802 | 9.19E-04 | | | Parkinson's disease | HPOID:0001300 | DOID:14330 | G | intron | GWASdb_trait |
| 18 | 71799576 | rs8086078 | G | C | rs8086078 | 7.20E-05 | | | Age-related macular degeneration | HPOID:0007868 | DOID:10871 | G | intron | GWASdb_trait |
| 18 | 71799576 | rs8086078 | G | C | rs8086078 | 3.24E-06 | | | Age-related macular degeneration | HPOID:0007868 | DOID:10871 | G | intron | GWASdb_trait |
| 18 | 71799576 | rs8086078 | G | C | rs8086078 | 1.26E-05 | | | Age-related macular degeneration | HPOID:0007868 | DOID:10871 | G | intron | GWASdb_trait |
| 18 | 71805503 | rs4556879 | C | T | rs4556879 | 9.75E-07 | | | Meningococcal disease | HPOID:0001287 | DOID:9931 | T,C | intron | GWASdb_trait |
| 18 | 71808441 | rs9319893 | A | C | rs9319893 | 8.58E-04 | | | Multiple complex diseases | HPOID:0000118 | NA | A | intron | GWASdb_trait |
| 18 | 71811235 | rs9952197 | G | A | rs9952197 | 1.47E-06 | | | Meningococcal disease | HPOID:0001287 | DOID:9931 | G,A | intron | GWASdb_trait |