Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2293088
rs2293088
Entrez Id: 339398
Gene Symbol: LINGO4
LINGO4
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1521179
rs1521179
Entrez Id: 339398
Gene Symbol: LINGO4
LINGO4
CUI: C0270736
Disease:
Essential Tremor
0.010 GeneticVariation BEFREE No significant differences in genotypic and allele distributions between patients and control subjects for rs61746299 and rs1521179 (p = 0.531 and p = 0.867 for genotypic distributions; p = 1.000 and p = 0.844 for allele distributions) were observed, suggesting variants in coding region of the LINGO4 gene may play litter or no role in the risk of ET susceptibility. 22104011 2012
dbSNP: rs61746299
rs61746299
Entrez Id: 339398
Gene Symbol: LINGO4
LINGO4
CUI: C0270736
Disease:
Essential Tremor
0.010 GeneticVariation BEFREE No significant differences in genotypic and allele distributions between patients and control subjects for rs61746299 and rs1521179 (p = 0.531 and p = 0.867 for genotypic distributions; p = 1.000 and p = 0.844 for allele distributions) were observed, suggesting variants in coding region of the LINGO4 gene may play litter or no role in the risk of ET susceptibility. 22104011 2012