Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.820 GeneticVariation BEFREE DNA was extracted from blood in order to analyse EBV and HHV-6 viral load by quantitative real-time polymerase chain reaction and to genotype MS-related single nucleotide polymorphisms (rs3135388, rs2248359 and rs12368653) when possible. 29996002 2018
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.820 GeneticVariation BEFREE In addition, we found difference in the genotype of rs12368653 between MS patients and controls (p=0.008). 25542806 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.820 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.820 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.820 GeneticVariation GWASDB Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. 19525955 2009