| Entry | The KEGG VARIANT database is a collection of human gene variants that can be associated with human diseases and drugs. Each variant is identified by the human gene ID followed by "v" and a number. |
|---|---|
| Name | Human gene variant name. |
| Type | Loss or gain of function. |
| Gene | Human gene name with KEGG Orthology (KO) information. |
| Organism | Currently, this field is always "hsa_var" for human gene variants. |
| Variation | Details of variations with links to outside databases. |
| Network | Network variation maps containing the human gene variant. |
| Disease | Diseases associated with the human gene variant. |
| Drug target | Known drugs targeting the human gene variant. |
| Reference | Original references used for defining the human gene variant. |
| LinkDB | 'All DBs' button in this field retrieves all available links to related database entries in the LinkDB system. At GenomeNet this field does not appear; instead a list of actual links is displayed on the right. |