Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10644
Gene Symbol: IGF2BP2
IGF2BP2
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007

Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876

2007

Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248

2007

Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. 17463249

2007

Entrez Id: 79068
Gene Symbol: FTO
FTO
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248

2007

Entrez Id: 79068
Gene Symbol: FTO
FTO
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007

Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.500 GeneticVariation GWASCAT 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 GWASCAT Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007

Entrez Id: 79068
Gene Symbol: FTO
FTO
CUI: C0028754
Disease: Obesity
Obesity
0.500 GeneticVariation GWASCAT Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants. 18159244

2007

Entrez Id: 4211
Gene Symbol: MEIS1
MEIS1
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome
0.500 GeneticVariation GWASCAT MEIS1 has been implicated in limb development, raising the possibility that RLS has components of a developmental disorder. 17637780

2007

Entrez Id: 4016
Gene Symbol: LOXL1
LOXL1
CUI: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome
0.500 GeneticVariation GWASCAT Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. 17690259

2007

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.500 GeneticVariation GWASCAT We identified four SNPs in intron 2 of FGFR2 (which encodes a receptor tyrosine kinase and is amplified or overexpressed in some breast cancers) that were highly associated with breast cancer and confirmed this association in 1,776 affected individuals and 2,072 controls from three additional studies. 17529973

2007

Entrez Id: 4046
Gene Symbol: LSP1
LSP1
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.500 GeneticVariation GWASCAT Genome-wide association study identifies novel breast cancer susceptibility loci. 17529967

2007

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.500 GeneticVariation GWASCAT Genome-wide association study identifies novel breast cancer susceptibility loci. 17529967

2007

Entrez Id: 3560
Gene Symbol: IL2RB
IL2RB
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.470 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007

Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
CUI: C0242216
Disease: Biliary calculi
Biliary calculi
0.420 GeneticVariation GWASCAT A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509

2007

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.410 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007

Entrez Id: 4092
Gene Symbol: SMAD7
SMAD7
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.410 GeneticVariation GWASCAT A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. 17934461

2007

Entrez Id: 79068
Gene Symbol: FTO
FTO
CUI: C0005910
Disease: Body Weight
Body Weight
0.400 GeneticVariation GWASCAT Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. 17658951

2007

Entrez Id: 9846
Gene Symbol: GAB2
GAB2
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.200 GeneticVariation GWASCAT GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. 17553421

2007

Entrez Id: 100048912
Gene Symbol: CDKN2B-AS1
CDKN2B-AS1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.200 GeneticVariation GWASCAT Genomewide association analysis of coronary artery disease. 17634449

2007

Entrez Id: 100048912
Gene Symbol: CDKN2B-AS1
CDKN2B-AS1
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.200 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007

Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
Diabetes Mellitus, Insulin-Dependent
0.200 GeneticVariation GWASCAT Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. 17554260

2007

Entrez Id: 2065
Gene Symbol: ERBB3
ERBB3
Diabetes Mellitus, Insulin-Dependent
0.200 GeneticVariation GWASCAT Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. 17554260

2007

Entrez Id: 10666
Gene Symbol: CD226
CD226
Diabetes Mellitus, Insulin-Dependent
0.200 GeneticVariation GWASCAT Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. 17554260

2007