Source: GWASCAT ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2066844
rs2066844
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
1.000 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs2066845
rs2066845
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
1.000 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs2066847
rs2066847
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
T 0.890 GeneticVariation GWASCAT Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233 2012
dbSNP: rs2066847
rs2066847
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
0.890 GeneticVariation GWASCAT Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. 20570966 2010
dbSNP: rs2066847
rs2066847
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
C 0.890 GeneticVariation GWASCAT Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
dbSNP: rs5743293
rs5743293
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
0.830 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs2076756
rs2076756
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
G 0.830 GeneticVariation GWASCAT A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669 2013
dbSNP: rs2076756
rs2076756
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
G 0.830 GeneticVariation GWASCAT A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388 2012
dbSNP: rs2076756
rs2076756
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
G 0.830 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463 2010
dbSNP: rs2076756
rs2076756
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
0.830 GeneticVariation GWASCAT Systematic association mapping identifies NELL1 as a novel IBD disease gene. 17684544 2007
dbSNP: rs2076756
rs2076756
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
0.830 GeneticVariation GWASCAT Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756 2007
dbSNP: rs2076756
rs2076756
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
0.820 GeneticVariation GWASCAT A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. 17068223 2006
dbSNP: rs17221417
rs17221417
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
G 0.810 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300 2007
dbSNP: rs5743289
rs5743289
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
0.810 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
dbSNP: rs5743289
rs5743289
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease
0.810 GeneticVariation GWASCAT Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789 2007
dbSNP: rs2066845
rs2066845
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0009324
Disease:
Ulcerative Colitis
0.800 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs5743289
rs5743289
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
T 0.800 GeneticVariation GWASCAT Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. 18758464 2008
dbSNP: rs2066844
rs2066844
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
0.790 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs2066845
rs2066845
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0038013
Disease:
Ankylosing spondylitis
0.730 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs2066845
rs2066845
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0033860
Disease:
Psoriasis
0.710 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs2066844
rs2066844
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0004096
Disease:
Asthma
T 0.700 GeneticVariation GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019
dbSNP: rs2066844
rs2066844
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0264408
Disease:
Childhood asthma
T 0.700 GeneticVariation GWASCAT Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. 31036433 2019
dbSNP: rs2066844
rs2066844
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0264408
Disease:
Childhood asthma
0.700 GeneticVariation GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019
dbSNP: rs2066844
rs2066844
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0149745
Disease:
Oral Ulcer
T 0.700 GeneticVariation GWASCAT Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. 30837455 2019
dbSNP: rs2066845
rs2066845
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0008313
Disease:
Cholangitis, Sclerosing
0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016