Source: GWASDB

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 		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 		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 		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 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 GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
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 		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 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 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
dbSNP: rs17824933
rs17824933
CD6
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.850 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
dbSNP: rs703842
rs703842
CYP27B1 ; METTL1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.840 GeneticVariation GWASDB Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. 19525955

2009
dbSNP: rs10492972
rs10492972
KIF1B
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		C 0.830 GeneticVariation GWASDB Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. 18997785

2008
dbSNP: rs9657904
rs9657904
CBLB ; LOC107986109
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		T 0.830 GeneticVariation GWASDB Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis. 20453840

2010
dbSNP: rs12368653
rs12368653
TSPAN31 ; AGAP2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.820 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs12368653
rs12368653
TSPAN31 ; AGAP2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.820 GeneticVariation GWASDB Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. 19525955

2009
dbSNP: rs180515
rs180515
RPS6KB1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.820 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs2248359
rs2248359
CYP24A1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.820 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs2300747
rs2300747
CD58 ; MIR548AC
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.820 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011
dbSNP: rs2300747
rs2300747
CD58 ; MIR548AC
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.820 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs2300747
rs2300747
CD58 ; MIR548AC
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		A 0.820 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
dbSNP: rs744166
rs744166
STAT3
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.820 GeneticVariation GWASDB SNP (rs744166) within the STAT3 gene was associated to MS (p = 2.75 x 10(-10), OR 0.87, confidence interval 0.83-0.91). 20159113

2010
dbSNP: rs9282641
rs9282641
CD86
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		G 0.820 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011