×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
Diabetes Mellitus, Non-Insulin-Dependent
1.000
GeneticVariation
GWASDB
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
24509480
2014
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
Malignant neoplasm of breast
1.000
GeneticVariation
GWASDB
Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
23535729
2013
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASDB
A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
22936669
2013
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
Diabetes Mellitus, Non-Insulin-Dependent
1.000
GeneticVariation
GWASDB
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India.
23300278
2013
×
Entrez Id:
6331
Gene Symbol:
SCN5A
SCN5A
Brugada Syndrome (disorder)
1.000
GeneticVariation
GWASDB
Common variants at SCN5A -SCN10A and HEY2 are associated with Brugada syndrome , a rare disease with high risk of sudden cardiac death.
23872634
2013
×
Entrez Id:
2099
Gene Symbol:
ESR1
ESR1
Malignant neoplasm of breast
1.000
GeneticVariation
GWASDB
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.
22976474
2012
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASDB
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
22412388
2012
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASDB
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
23128233
2012
×
Entrez Id:
3064
Gene Symbol:
HTT
HTT
Huntington Disease
1.000
GeneticVariation
GWASDB
Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.
22387017
2012
×
Entrez Id:
5621
Gene Symbol:
PRNP
PRNP
Creutzfeldt-Jakob disease
1.000
GeneticVariation
GWASDB
Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.
22137330
2012
×
Entrez Id:
3172
Gene Symbol:
HNF4A
HNF4A
Diabetes Mellitus, Non-Insulin-Dependent
1.000
GeneticVariation
GWASDB
In the combined analysis, we identified common genetic variants at six loci (GRB14, ST6GAL1, VPS26A, HMG20A, AP3S2 and HNF4A ) newly associated with T2D (P = 4.1 × 10(-8) to P = 1.9 × 10(-11)).
21874001
2011
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASDB
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
21102463
2010
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASDB
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.
20570966
2010
×
Entrez Id:
5621
Gene Symbol:
PRNP
PRNP
Creutzfeldt-Jakob disease
1.000
GeneticVariation
GWASDB
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
19081515
2009
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASDB
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
18587394
2008
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
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:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASDB
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
GWASDB
A proportion of these were replicated in two independent German Caucasian samples, including the established CD loci NOD2 and IBD5.
17804789
2007
×
Entrez Id:
64127
Gene Symbol:
NOD2
NOD2
Crohn Disease
1.000
GeneticVariation
GWASDB
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
GWASDB
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
GWASDB
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
17068223
2006
×
Entrez Id:
3767
Gene Symbol:
KCNJ11
KCNJ11
Diabetes Mellitus, Non-Insulin-Dependent
0.900
GeneticVariation
GWASDB
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
24509480
2014
×
Entrez Id:
3767
Gene Symbol:
KCNJ11
KCNJ11
Diabetes Mellitus, Non-Insulin-Dependent
0.900
GeneticVariation
GWASDB
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India.
23300278
2013
×
Entrez Id:
2645
Gene Symbol:
GCK
GCK
Diabetes Mellitus, Non-Insulin-Dependent
0.900
GeneticVariation
GWASDB
New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population.
23575436
2013
×
Entrez Id:
3664
Gene Symbol:
IRF6
IRF6
Cleft upper lip
0.900
GeneticVariation
GWASDB
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.
22863734
2012