×
Entrez Id:
3075
Gene Symbol:
CFH
CFH
Age related macular degeneration
0.500
GeneticVariation
GWASCAT
The CFH gene is located on chromosome 1 in a region repeatedly linked to AMD in family-based studies.
15761122
2005
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Inflammatory Bowel Diseases
0.500
GeneticVariation
GWASCAT
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
17068223
2006
×
Entrez Id:
5654
Gene Symbol:
HTRA1
HTRA1
Age related macular degeneration
0.500
GeneticVariation
GWASCAT
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:
9722
Gene Symbol:
NOS1AP
NOS1AP
QT interval feature (observable entity)
0.100
GeneticVariation
GWASCAT
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
16648850
2006
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASCAT
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
17684544
2007
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASCAT
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
17554300
2007
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASCAT
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.
17447842
2007
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASCAT
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
17435756
2007
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASCAT
A proportion of these were replicated in two independent German Caucasian samples, including the established CD loci NOD2 and IBD5.
17804789
2007
×
Entrez Id:
26191
Gene Symbol:
PTPN22
PTPN22
Diabetes Mellitus, Insulin-Dependent
0.900
GeneticVariation
GWASCAT
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.
17554260
2007
×
Entrez Id:
26191
Gene Symbol:
PTPN22
PTPN22
Diabetes Mellitus, Insulin-Dependent
0.900
GeneticVariation
GWASCAT
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.
17632545
2007
×
Entrez Id:
3767
Gene Symbol:
KCNJ11
KCNJ11
Diabetes Mellitus, Non-Insulin-Dependent
0.900
GeneticVariation
GWASCAT
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
17463246
2007
×
Entrez Id:
3767
Gene Symbol:
KCNJ11
KCNJ11
Diabetes Mellitus, Non-Insulin-Dependent
0.900
GeneticVariation
GWASCAT
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
17463248
2007
×
Entrez Id:
3767
Gene Symbol:
KCNJ11
KCNJ11
Diabetes Mellitus, Non-Insulin-Dependent
0.900
GeneticVariation
GWASCAT
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.
17463249
2007
×
Entrez Id:
26191
Gene Symbol:
PTPN22
PTPN22
Rheumatoid Arthritis
0.700
GeneticVariation
GWASCAT
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.
17804836
2007
×
Entrez Id:
345611
Gene Symbol:
IRGM
IRGM
Crohn Disease
0.700
GeneticVariation
GWASCAT
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
17554300
2007
×
Entrez Id:
149233
Gene Symbol:
IL23R
IL23R
Crohn Disease
0.700
GeneticVariation
GWASCAT
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.
17447842
2007
×
Entrez Id:
149233
Gene Symbol:
IL23R
IL23R
Crohn Disease
0.700
GeneticVariation
GWASCAT
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
17554300
2007
×
Entrez Id:
149233
Gene Symbol:
IL23R
IL23R
Crohn Disease
0.700
GeneticVariation
GWASCAT
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
17804789
2007
×
Entrez Id:
149233
Gene Symbol:
IL23R
IL23R
Crohn Disease
0.700
GeneticVariation
GWASCAT
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
17435756
2007
×
Entrez Id:
55054
Gene Symbol:
ATG16L1
ATG16L1
Crohn Disease
0.700
GeneticVariation
GWASCAT
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
17554300
2007
×
Entrez Id:
55054
Gene Symbol:
ATG16L1
ATG16L1
Crohn Disease
0.700
GeneticVariation
GWASCAT
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
17435756
2007
×
Entrez Id:
6934
Gene Symbol:
TCF7L2
TCF7L2
Diabetes Mellitus, Non-Insulin-Dependent
0.700
GeneticVariation
GWASCAT
We conducted a genome-wide association study for type 2 diabetes (T2D ) in Icelandic cases and controls, and we found that a previously described variant in the transcription factor 7-like 2 gene (TCF7L2 ) gene conferred the most significant risk.
17460697
2007
×
Entrez Id:
6934
Gene Symbol:
TCF7L2
TCF7L2
Diabetes Mellitus, Non-Insulin-Dependent
0.700
GeneticVariation
GWASCAT
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
17463248
2007
×
Entrez Id:
54901
Gene Symbol:
CDKAL1
CDKAL1
Diabetes Mellitus, Non-Insulin-Dependent
0.700
GeneticVariation
GWASCAT
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
17554300
2007