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 | 14 | 69604244 | rs8008735 | A | C | rs8008735 | 8.66E-04 | | | Amyotrophic lateral sclerosis (sporadic) | HPOID:0007354 | DOID:332 | A | intron | GWASdb_trait | 14 | 69619173 | rs1275419 | A | C | rs1275419 | 9.77E-05 | | | Coronary heart disease | HPOID:0001677 | DOID:3393 | C | intron | GWASdb_trait | |