|Dataset||GWASdb SNP-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the disease essential tremor in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
|SLC1A2||solute carrier family 1 (glial high affinity glutamate transporter), member 2||1.31635|