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 |
5 | 40767397 | rs1002424 | A | G | rs1002424 | 5.21E-10 | | | Schizophrenia | HPOID:0100753 | DOID:5419 | T | intron | GWASdb_trait |
5 | 40775297 | rs3792822 | C | T | rs3792822 | 9.80E-04 | | | Major depressive disorder | HPOID:0000716 | DOID:1470 | G | intron | GWASdb_trait |
5 | 40790551 | rs10074991 | G | A | rs10074991 | 2.54E-04 | | | Multiple complex diseases | HPOID:0000118 | NA | A | intron | GWASdb_trait |
5 | 40790551 | rs10074991 | G | A | rs10074991 | 7.10E-04 | | | Major depressive disorder | HPOID:0000716 | DOID:1470 | A | intron | GWASdb_trait |
5 | 40790551 | rs10074991 | G | A | rs10074991 | 1.94E-04 | | | Autism spectrum disorders (language delay) | HPOID:0000729 | DOID:0060041 | A | intron | GWASdb_trait |
5 | 40790551 | rs10074991 | G | A | rs10074991 | 5.11E-05 | | | Parkinson's disease | HPOID:0001300 | DOID:14330 | A | intron | GWASdb_trait |
5 | 40790551 | rs10074991 | G | A | rs10074991 | 4.21E-10 | | | Schizophrenia | HPOID:0100753 | DOID:5419 | A | intron | GWASdb_trait |
5 | 40791884 | rs13361707 | C | T | rs13361707 | 2.25E-04 | | | Multiple complex diseases | HPOID:0000118 | NA | C | intron | GWASdb_trait |
5 | 40791884 | rs13361707 | C | T | rs13361707 | 6.80E-04 | | | Major depressive disorder | HPOID:0000716 | DOID:1470 | C | intron | GWASdb_trait |
5 | 40791884 | rs13361707 | C | T | rs13361707 | 2.30E-05 | | | Urinary metabolites | HPOID:0000079 | DOID:557 | C | intron | GWASdb_trait |
5 | 40791884 | rs13361707 | C | T | rs13361707 | 8.00E-29 | | | Gastric cancer | HPOID:0012126 | DOID:3717 | C | intron | GWASdb_trait |
5 | 40791884 | rs13361707 | C | T | rs13361707 | 7.77E-08 | | | Schizophrenia | HPOID:0100753 | DOID:5419 | C | intron | GWASdb_trait |