Essential tremor Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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 https://www.ebi.ac.uk/gwas/search?query=Essential tremor
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Genes

2 genes associated with the Essential tremor phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
LINGO1 leucine rich repeat and Ig domain containing 1 0.522843
SLC1A2 solute carrier family 1 (glial high affinity glutamate transporter), member 2 0.342586