rs11856808
This is a intron variant variant in the LINGO1 gene.
▶Research that mentions this SNP (3)
▶LINGO1 polymorphisms are associated with essential tremor in EuropeansAssociationN=542Sandra Thier et al.(2010)· Movement Disorders
Case-control study of 542 Taiwanese subjects (273 ET patients, 269 controls) demonstrating association of the SLC1A2 rs3794087 A allele with essential tremor (OR=1.37, 95% CI 1.02-1.86, p=0.03), confirming a previous European GWAS finding in an Asian population.
▶Role of LINGO1 polymorphisms in Parkinson's diseaseAssociationN=694Dietrich Haubenberger et al.(2009)· Movement Disorders
This case-control study examined whether LINGO1 gene variants (rs9652490, rs11856808, rs7177008) associated with essential tremor also confer risk for Parkinson's disease in an Austrian population of 349 PD patients and 345 controls. No significant associations were found between any LINGO1 SNP genotypes or alleles and PD (rs9652490 p=0.61), nor in the subgroup of tremor-dominant PD patients (n=34, p=0.76). The findings argue against a major role of LINGO1 variants in PD susceptibility despite the documented clinical overlap between the two disorders.
▶Alpha‐synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan populationAssociationN=694Alex Rajput et al.(2009)· Movement Disorders
This case-control study investigated whether LINGO1 gene polymorphisms associated with essential tremor also confer risk for Parkinson's disease (PD). Three SNPs (rs9652490, rs11856808, rs7177008) were genotyped in 349 PD patients and 345 controls from Austria. No significant associations were found between any LINGO1 variants and PD risk overall (p=0.61 for rs9652490) or in tremor-dominant PD patients, arguing against a major role of LINGO1 variants in PD susceptibility.
About LINGO1
Predicted to enable epidermal growth factor receptor binding activity. Predicted to act upstream of or within negative regulation of oligodendrocyte differentiation; negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and neuron development. Predicted to be located in plasma membrane. Predicted to be active in several cellular components, including extracellular space; glutamatergic synapse; and presynapse. Implicated in autosomal recessive intellectual developmental disorder 64 and glaucoma. [provided by Alliance of Genome Resources, Jul 2025]
View all LINGO1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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