rs2066844
|
|
Crohn Disease
|
|
1.000 |
GeneticVariation
|
GWASDB |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
rs2066844
|
|
Crohn Disease
|
|
1.000 |
GeneticVariation
|
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
rs2066845
|
|
Crohn Disease
|
|
1.000 |
GeneticVariation
|
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
rs2066845
|
|
Crohn Disease
|
|
1.000 |
GeneticVariation
|
GWASDB |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
rs2066845
|
|
Crohn Disease
|
|
1.000 |
GeneticVariation
|
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
rs11209026
|
|
Crohn Disease
|
G |
0.900 |
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 |
rs11209026
|
|
Crohn Disease
|
G |
0.900 |
GeneticVariation
|
GWASDB |
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
|
22412388 |
2012 |
rs11209026
|
|
Crohn Disease
|
|
0.900 |
GeneticVariation
|
GWASDB |
One is SNP rs11209026 in exon 9 of IL23R for association with Crohn's disease, which is predicted to be probably damaging by PolyPhen2.
|
22293688 |
2012 |
rs11209026
|
|
Crohn Disease
|
G |
0.900 |
GeneticVariation
|
GWASDB |
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
|
21102463 |
2010 |
rs11209026
|
|
Crohn Disease
|
|
0.900 |
GeneticVariation
|
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
rs11209026
|
|
Crohn Disease
|
|
0.900 |
GeneticVariation
|
GWASDB |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
rs11209026
|
|
Crohn Disease
|
|
0.900 |
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 |
rs11209026
|
|
Crohn Disease
|
|
0.900 |
GeneticVariation
|
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
rs2241880
|
|
Crohn Disease
|
G |
0.900 |
GeneticVariation
|
GWASDB |
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
|
22412388 |
2012 |
rs2241880
|
|
Crohn Disease
|
|
0.900 |
GeneticVariation
|
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
rs2241880
|
|
Crohn Disease
|
|
0.900 |
GeneticVariation
|
GWASDB |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
rs2241880
|
|
Crohn Disease
|
G |
0.900 |
GeneticVariation
|
GWASDB |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
rs2066847
|
|
Crohn Disease
|
T |
0.890 |
GeneticVariation
|
GWASDB |
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
|
23128233 |
2012 |
rs2066847
|
|
Crohn Disease
|
|
0.890 |
GeneticVariation
|
GWASDB |
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.
|
20570966 |
2010 |
rs2066847
|
|
Crohn Disease
|
C |
0.890 |
GeneticVariation
|
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
rs2066847
|
|
Crohn Disease
|
|
0.890 |
GeneticVariation
|
GWASDB |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
rs2542151
|
|
Crohn Disease
|
|
0.880 |
GeneticVariation
|
GWASDB |
A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease.
|
21298027 |
2011 |
rs2542151
|
|
Crohn Disease
|
G |
0.880 |
GeneticVariation
|
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
rs2542151
|
|
Crohn Disease
|
|
0.880 |
GeneticVariation
|
GWASDB |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
rs2542151
|
|
Crohn Disease
|
G |
0.880 |
GeneticVariation
|
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |