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rs11856808

From SNPedia

Orientationplus
Stabilizedplus
Make rs11856808(C;C)
Make rs11856808(C;T)
Make rs11856808(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position77680428
GeneLINGO1
is asnp
is mentioned by
dbSNPrs11856808
ebirs11856808
HLIrs11856808
Exacrs11856808
Varsomers11856808
Maprs11856808
PheGenIrs11856808
hapmaprs11856808
1000 genomesrs11856808
hgdprs11856808
ensemblrs11856808
gopubmedrs11856808
geneviewrs11856808
scholarrs11856808
googlers11856808
pharmgkbrs11856808
gwascentralrs11856808
openSNPrs11856808
23andMers11856808
23andMe allrs11856808
SNP Nexus

SNPshotrs11856808
SNPdbers11856808
MSV3drs11856808
GWAS Ctlgrs11856808
GMAF0.4362
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19908305OA-icon.png] Role of LINGO1 polymorphisms in Parkinson's disease


[PMID 20310002] LINGO1 polymorphisms are associated with essential tremor in Europeans


[PMID 20600614] Screening for two SNPs of LINGO1 gene in patients with essential tremor or sporadic Parkinson's disease in Chinese population.


[PMID 21207446] LINGO1 gene analysis in Parkinson's disease phenotypes.


[PMID 21219542] Lack of association of LINGO1 rs9652490 and rs11856808 SNPs with familial essential tremor.


[PMID 21955595] LINGO1 rs9652490 and rs11856808 are not associated with the risk of Parkinson's disease: results of a meta-analysis.


[PMID 22425540] LINGO1 and risk for essential tremor: results of a meta-analysis of rs9652490 and rs11856808.


[PMID 23574883OA-icon.png] LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis