Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2104286
rs2104286
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.900 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602

2013
dbSNP: rs2104286
rs2104286
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.900 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011
dbSNP: rs2104286
rs2104286
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		T 0.900 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
dbSNP: rs2104286
rs2104286
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		T 0.900 GeneticVariation GWASCAT Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
dbSNP: rs2104286
rs2104286
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.900 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
dbSNP: rs6897932
rs6897932
IL7R
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.900 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs6897932
rs6897932
IL7R
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.900 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs6897932
rs6897932
IL7R
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.900 GeneticVariation GWASCAT Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
dbSNP: rs6897932
rs6897932
IL7R
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.900 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
dbSNP: rs3135388
rs3135388
HLA-DRA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.890 GeneticVariation GWASCAT Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. 25616667

2015
dbSNP: rs3135388
rs3135388
HLA-DRA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.890 GeneticVariation GWASCAT Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
dbSNP: rs3135388
rs3135388
HLA-DRA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.890 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
dbSNP: rs3135388
rs3135388
HLA-DRA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.890 GeneticVariation GWASCAT Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
dbSNP: rs3135388
rs3135388
HLA-DRA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.890 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.880 GeneticVariation GWASCAT Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. 27386562

2016
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.880 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602

2013
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.880 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.880 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.880 GeneticVariation GWASCAT Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
dbSNP: rs1800693
rs1800693
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.880 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
dbSNP: rs12722489
rs12722489
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.850 GeneticVariation GWASCAT Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011
dbSNP: rs12722489
rs12722489
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.850 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011
dbSNP: rs12722489
rs12722489
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.850 GeneticVariation GWASCAT Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
dbSNP: rs12722489
rs12722489
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.850 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
dbSNP: rs17824933
rs17824933
CD6
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.850 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011