Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 965
Gene Symbol: CD58
CD58
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASDB No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. 24234648

2014

Entrez Id: 3126
Gene Symbol: HLA-DRB4
HLA-DRB4
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.110 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.110 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

Entrez Id: 64084
Gene Symbol: CLSTN2
CLSTN2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

Entrez Id: 6041
Gene Symbol: RNASEL
RNASEL
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB A genome-wide association study of brain lesion distribution in multiple sclerosis. 23412934

2013

Entrez Id: 9639
Gene Symbol: ARHGEF10
ARHGEF10
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB A genome-wide association study of brain lesion distribution in multiple sclerosis. 23412934

2013

Entrez Id: 3128
Gene Symbol: HLA-DRB6
HLA-DRB6
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

Entrez Id: 100288077
Gene Symbol: WTAPP1
WTAPP1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB A genome-wide association study of brain lesion distribution in multiple sclerosis. 23412934

2013

Entrez Id: 101929163
Gene Symbol: TSBP1-AS1
TSBP1-AS1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

Entrez Id: 57531
Gene Symbol: HACE1
HACE1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB A genome-wide association study of brain lesion distribution in multiple sclerosis. 23412934

2013

Entrez Id: 284677
Gene Symbol: SNHG28
SNHG28
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

Entrez Id: 8575
Gene Symbol: PRKRA
PRKRA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

Entrez Id: 101927027
Gene Symbol: CHROMR
CHROMR
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

Entrez Id: 101929163
Gene Symbol: TSBP1-AS1
TSBP1-AS1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB A genome-wide association study in progressive multiple sclerosis. 22457343

2012

Entrez Id: 10665
Gene Symbol: TSBP1
TSBP1
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.100 GeneticVariation GWASDB A genome-wide association study in progressive multiple sclerosis. 22457343

2012

Entrez Id: 3575
Gene Symbol: IL7R
IL7R
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011

Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011

Entrez Id: 965
Gene Symbol: CD58
CD58
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011

Entrez Id: 23274
Gene Symbol: CLEC16A
CLEC16A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011

Entrez Id: 7132
Gene Symbol: TNFRSF1A
TNFRSF1A
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011

Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011

Entrez Id: 965
Gene Symbol: CD58
CD58
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011

Entrez Id: 958
Gene Symbol: CD40
CD40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011

Entrez Id: 6775
Gene Symbol: STAT4
STAT4
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.430 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011

Entrez Id: 8740
Gene Symbol: TNFSF14
TNFSF14
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.420 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011