| Dataset | GWASdb SNP-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A movement disorder that causes involuntary tremors, especially in the hands. It occurs alone without other neurological signs and symptoms. (Human Disease Ontology, DOID_4990) |
| External Link | http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:4990 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the disease essential tremor in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| SLC1A2 | solute carrier family 1 (glial high affinity glutamate transporter), member 2 | 1.31635 |
