×
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:
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:
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:
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:
6934
Gene Symbol:
TCF7L2
TCF7L2
Diabetes Mellitus, Non-Insulin-Dependent
0.700
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 identifies novel risk loci for type 2 diabetes.
17293876
2007
×
Entrez Id:
100750225
Gene Symbol:
PCAT1
PCAT1
Prostate carcinoma
0.200
GeneticVariation
GWASCAT
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.
17401363
2007
×
Entrez Id:
5462
Gene Symbol:
POU5F1B
POU5F1B
Prostate carcinoma
0.150
GeneticVariation
GWASCAT
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.
17401363
2007
×
Entrez Id:
101805488
Gene Symbol:
CCAT2
CCAT2
Prostate carcinoma
0.110
GeneticVariation
GWASCAT
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.
17401363
2007
×
Entrez Id:
727677
Gene Symbol:
CASC8
CASC8
Prostate carcinoma
0.100
GeneticVariation
GWASCAT
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.
17401363
2007
×
Entrez Id:
100750225
Gene Symbol:
PCAT1
PCAT1
Prostate carcinoma
0.200
GeneticVariation
GWASCAT
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
17401366
2007
×
Entrez Id:
101867536
Gene Symbol:
PRNCR1
PRNCR1
Prostate carcinoma
0.170
GeneticVariation
GWASCAT
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
17401366
2007
×
Entrez Id:
727677
Gene Symbol:
CASC8
CASC8
Prostate carcinoma
0.100
GeneticVariation
GWASCAT
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
17401366
2007
×
Entrez Id:
103021165
Gene Symbol:
CASC19
CASC19
Prostate carcinoma
0.100
GeneticVariation
GWASCAT
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
17401366
2007
×
Entrez Id:
3613
Gene Symbol:
IMPA2
IMPA2
Cerebrovascular accident
0.100
GeneticVariation
GWASCAT
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.
17434096
2007
×
Entrez Id:
79068
Gene Symbol:
FTO
FTO
Body mass index
0.100
GeneticVariation
GWASCAT
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
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:
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 identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
17435756
2007
C1orf141
Crohn Disease
0.100
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
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
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:
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:
54901
Gene Symbol:
CDKAL1
CDKAL1
Diabetes Mellitus, Non-Insulin-Dependent
0.700
GeneticVariation
GWASCAT
In addition to confirming two recently identified risk variants, we identified a variant in the CDKAL1 gene that was associated with T2D in individuals of European ancestry (allele-specific odds ratio (OR) = 1.20 (95% confidence interval, 1.13-1.27), P = 7.7 x 10(-9)) and individuals from Hong Kong of Han Chinese ancestry (OR = 1.25 (1.11-1.40), P = 0.00018).
17460697
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