Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26191
Gene Symbol: PTPN22
PTPN22
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis. 17159887

2007
Entrez Id: 10665
Gene Symbol: TSBP1
TSBP1
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.130 GeneticVariation GWASDB Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis. 17159887

2007
Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.120 GeneticVariation GWASDB Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis. 17159887

2007
Entrez Id: 101929163
Gene Symbol: TSBP1-AS1
TSBP1-AS1
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.100 GeneticVariation GWASDB Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis. 17159887

2007
Entrez Id: 5583
Gene Symbol: PRKCH
PRKCH
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.170 GeneticVariation GWASDB A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. 17206144

2007
Entrez Id: 3699
Gene Symbol: ITIH3
ITIH3
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.110 GeneticVariation GWASDB Furthermore, we found expression of the ITIH3 protein in the vascular smooth muscle cells and macrophages in the human atherosclerotic lesions, suggesting ITIH3 SNP to be a novel genetic risk factor of MI. 17211523

2007
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876

2007
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.500 GeneticVariation GWASDB A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876

2007
Entrez Id: 23261
Gene Symbol: CAMTA1
CAMTA1
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.110 GeneticVariation GWASDB A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876

2007
Entrez Id: 10891
Gene Symbol: PPARGC1A
PPARGC1A
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.490 GeneticVariation GWASDB Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. 17362836

2007
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.100 GeneticVariation GWASDB Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. 17362836

2007
Entrez Id: 6334
Gene Symbol: SCN8A
SCN8A
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.100 GeneticVariation GWASDB Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. 17362836

2007
Entrez Id: 9674
Gene Symbol: KIAA0040
KIAA0040
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.100 GeneticVariation GWASDB Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. 17362836

2007
Entrez Id: 100750225
Gene Symbol: PCAT1
PCAT1
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.500 GeneticVariation GWASDB Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. 17401363

2007
Entrez Id: 5462
Gene Symbol: POU5F1B
POU5F1B
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.140 GeneticVariation GWASDB Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. 17401363

2007
Entrez Id: 101805488
Gene Symbol: CCAT2
CCAT2
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.110 GeneticVariation GWASDB Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. 17401363

2007
Entrez Id: 727677
Gene Symbol: CASC8
CASC8
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.100 GeneticVariation GWASDB Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. 17401363

2007
Entrez Id: 100750225
Gene Symbol: PCAT1
PCAT1
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.500 GeneticVariation GWASDB Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. 17401366

2007
Entrez Id: 103021165
Gene Symbol: CASC19
CASC19
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.100 GeneticVariation GWASDB Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. 17401366

2007
Entrez Id: 727677
Gene Symbol: CASC8
CASC8
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.100 GeneticVariation GWASDB Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. 17401366

2007
Entrez Id: 3613
Gene Symbol: IMPA2
IMPA2
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.100 GeneticVariation GWASDB A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. 17434096

2007
Entrez Id: 79068
Gene Symbol: FTO
FTO
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.100 GeneticVariation GWASDB A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. 17434869

2007
Entrez Id: 79068
Gene Symbol: FTO
FTO
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.100 GeneticVariation GWASDB A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. 17434869

2007
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation GWASDB Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756

2007
Entrez Id: 149233
Gene Symbol: IL23R
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASDB Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756

2007