Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 285830
Gene Symbol: HLA-F-AS1
HLA-F-AS1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 5460
Gene Symbol: POU5F1
POU5F1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 6046
Gene Symbol: BRD2
BRD2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 285834
Gene Symbol: HCG22
HCG22
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 10919
Gene Symbol: EHMT2
EHMT2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 6941
Gene Symbol: TCF19
TCF19
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 105375015
Gene Symbol: LINC02571
LINC02571
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 1041
Gene Symbol: CDSN
CDSN
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3778
Gene Symbol: KCNMA1
KCNMA1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 717
Gene Symbol: C2
C2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 401250
Gene Symbol: MCCD1
MCCD1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 1589
Gene Symbol: CYP21A2
CYP21A2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 10866
Gene Symbol: HCP5
HCP5
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 101929163
Gene Symbol: TSBP1-AS1
TSBP1-AS1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3108
Gene Symbol: HLA-DMA
HLA-DMA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 23095
Gene Symbol: KIF1B
KIF1B
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.460 GeneticVariation GWASDB KIF1B is a neuronally expressed gene plausibly implicated in the irreversible axonal loss characterizing MS in the long term. 18997785

2008
Entrez Id: 101929163
Gene Symbol: TSBP1-AS1
TSBP1-AS1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms. 18941528

2008
Entrez Id: 10665
Gene Symbol: TSBP1
TSBP1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms. 18941528

2008
Entrez Id: 965
Gene Symbol: CD58
CD58
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.500 GeneticVariation GWASDB We also replicated several known MS associations (HLA-DR15, P = 7.0 x 10(-184); CD58, P = 9.6 x 10(-8); EVI5-RPL5, P = 2.5 x 10(-6); IL2RA, P = 7.4 x 10(-6); CLEC16A, P = 1.1 x 10(-4); IL7R, P = 1.3 x 10(-3); TYK2, P = 3.5 x 10(-3)) and observed a statistical interaction between SNPs in EVI5-RPL5 and HLA-DR15 (P = 0.001). 19525955

2009
Entrez Id: 965
Gene Symbol: CD58
CD58
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.500 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.500 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.500 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009
Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.500 GeneticVariation GWASDB Replication in an independent set of 2,215 subjects with MS and 2,116 control subjects validates new MS susceptibility loci at TNFRSF1A (combined P = 1.59 x 10(-11)), IRF8 (P = 3.73 x 10(-9)) and CD6 (P = 3.79 x 10(-9)). 19525953

2009
Entrez Id: 923
Gene Symbol: CD6
CD6
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.420 GeneticVariation GWASDB Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. 19525953

2009