Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23327
Gene Symbol: NEDD4L
NEDD4L
CUI: C0004096
Disease: Asthma
Asthma 		0.110 GeneticVariation GWASDB A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. 11022011

2000
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.500 GeneticVariation GWASDB The CFH gene is located on chromosome 1 in a region repeatedly linked to AMD in family-based studies. 15761122

2005
Entrez Id: 9966
Gene Symbol: TNFSF15
TNFSF15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.200 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
Entrez Id: 944
Gene Symbol: TNFSF8
TNFSF8
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
Entrez Id: 50514
Gene Symbol: DELEC1
DELEC1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.100 GeneticVariation GWASDB A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. 16648850

2006
Entrez Id: 6239
Gene Symbol: RREB1
RREB1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.110 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 441250
Gene Symbol: TYW1B
TYW1B
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 9811
Gene Symbol: CTIF
CTIF
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 64215
Gene Symbol: DNAJC1
DNAJC1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 92949
Gene Symbol: ADAMTSL1
ADAMTSL1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 440279
Gene Symbol: UNC13C
UNC13C
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 442524
Gene Symbol: DPY19L2P3
DPY19L2P3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 374491
Gene Symbol: TPTE2P6
TPTE2P6
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 29119
Gene Symbol: CTNNA3
CTNNA3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 55529
Gene Symbol: PIP4P2
PIP4P2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.100 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657

2006
Entrez Id: 387715
Gene Symbol: ARMS2
ARMS2
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.700 GeneticVariation GWASDB HTRA1 promoter polymorphism in wet age-related macular degeneration. 17053108

2006
Entrez Id: 5654
Gene Symbol: HTRA1
HTRA1
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.500 GeneticVariation GWASDB Here we report that a single-nucleotide polymorphism in the promoter region of HTRA1, a serine protease gene on chromosome 10q26, is a major genetic risk factor for wet AMD. 17053108

2006
Entrez Id: 440823
Gene Symbol: MIAT
MIAT
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.500 GeneticVariation GWASDB These results indicate that the altered expression of MIAT by the SNP may play some role in the pathogenesis of MI. 17066261

2006
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006
Entrez Id: 149233
Gene Symbol: IL23R
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006
Entrez Id: 149233
Gene Symbol: IL23R
IL23R
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.500 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.500 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006
Entrez Id: 400757
Gene Symbol: C1orf141
C1orf141
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006
Entrez Id: 400757
Gene Symbol: C1orf141
C1orf141
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.100 GeneticVariation GWASDB A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223

2006