|
IRF1-AS1
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
|
RTEL1-TNFRSF6B
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
|
| Entrez Id: |
54901 |
| Gene Symbol: |
CDKAL1 |
CDKAL1
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
|
| Entrez Id: |
107984474 |
| Gene Symbol: |
LRRK2-DT |
LRRK2-DT
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
|
18587394 |
2008 |
|
| Entrez Id: |
645740 |
| Gene Symbol: |
NOS2P1 |
NOS2P1
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
26031 |
| Gene Symbol: |
OSBPL3 |
OSBPL3
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
275 |
| Gene Symbol: |
AMT |
AMT
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
327 |
| Gene Symbol: |
APEH |
APEH
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
C1orf141
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
|
LINC01475
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
|
| Entrez Id: |
387 |
| Gene Symbol: |
RHOA |
RHOA
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
LINC01475
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
| Entrez Id: |
2869 |
| Gene Symbol: |
GRK5 |
GRK5
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
6988 |
| Gene Symbol: |
TCTA |
TCTA
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
54828 |
| Gene Symbol: |
BCAS3 |
BCAS3
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
85407 |
| Gene Symbol: |
NKD1 |
NKD1
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
MIR3936HG
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
C1orf141
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
IRF1-AS1
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
C1orf141
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
| Entrez Id: |
374618 |
| Gene Symbol: |
TEX9 |
TEX9
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
| Entrez Id: |
84276 |
| Gene Symbol: |
NICN1 |
NICN1
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.
|
17804789 |
2007 |
|
C1orf141
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
|
17068223 |
2006 |
|
| Entrez Id: |
944 |
| Gene Symbol: |
TNFSF8 |
TNFSF8
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.
|
16221758 |
2005 |
|
| Entrez Id: |
50514 |
| Gene Symbol: |
DELEC1 |
DELEC1
|
Crohn Disease
|
0.100 |
GeneticVariation |
GWASDB |
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.
|
16221758 |
2005 |