Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.500 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.500 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3575
Gene Symbol: IL7R
IL7R
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.500 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3122
Gene Symbol: HLA-DRA
HLA-DRA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.440 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3117
Gene Symbol: HLA-DQA1
HLA-DQA1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.200 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.200 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 6891
Gene Symbol: TAP2
TAP2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.150 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.130 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3118
Gene Symbol: HLA-DQA2
HLA-DQA2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.110 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 3109
Gene Symbol: HLA-DMB
HLA-DMB
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.110 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 629
Gene Symbol: CFB
CFB
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.110 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.110 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007
Entrez Id: 10665
Gene Symbol: TSBP1
TSBP1
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: 29119
Gene Symbol: CTNNA3
CTNNA3
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: 7917
Gene Symbol: BAG6
BAG6
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: 7916
Gene Symbol: PRRC2A
PRRC2A
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: 26289
Gene Symbol: AK5
AK5
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: 3132
Gene Symbol: HLA-DRB9
HLA-DRB9
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: 8449
Gene Symbol: DHX16
DHX16
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: 677820
Gene Symbol: SNORA38
SNORA38
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: 170679
Gene Symbol: PSORS1C1
PSORS1C1
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: 401247
Gene Symbol: LINC00243
LINC00243
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: 7148
Gene Symbol: TNXB
TNXB
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: 100287272
Gene Symbol: USP8P1
USP8P1
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: 3134
Gene Symbol: HLA-F
HLA-F
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007