rs2241880
|
|
Crohn Disease
|
G |
0.900 |
GeneticVariation
|
GWASCAT |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
rs7517847
|
|
Crohn Disease
|
|
0.880 |
GeneticVariation
|
GWASCAT |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
rs2076756
|
|
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 |
rs224136
|
|
Crohn Disease
|
|
0.810 |
GeneticVariation
|
GWASCAT |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
rs11209026
|
|
Crohn Disease
|
|
0.900 |
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 |
rs5743289
|
|
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 |
rs1373692
|
|
Crohn Disease
|
|
0.800 |
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 |
rs2542151
|
|
Crohn Disease
|
|
0.880 |
GeneticVariation
|
GWASCAT |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
rs13361189
|
|
Crohn Disease
|
|
0.850 |
GeneticVariation
|
GWASCAT |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
rs10883365
|
|
Crohn Disease
|
|
0.830 |
GeneticVariation
|
GWASCAT |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
rs9858542
|
|
Crohn Disease
|
|
0.810 |
GeneticVariation
|
GWASCAT |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
rs9292777
|
|
Crohn Disease
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
rs2836754
|
|
Crohn Disease
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
rs12035082
|
|
Crohn Disease
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
|
17554261 |
2007 |
rs10801047
|
|
Crohn Disease
|
|
0.800 |
GeneticVariation
|
GWASCAT |
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
|
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
rs1000113
|
|
Crohn Disease
|
T |
0.840 |
GeneticVariation
|
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
rs10883365
|
|
Crohn Disease
|
G |
0.830 |
GeneticVariation
|
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
rs9858542
|
|
Crohn Disease
|
A |
0.810 |
GeneticVariation
|
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
rs17234657
|
|
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 |
rs17221417
|
|
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 |
rs11805303
|
|
Crohn Disease
|
T |
0.810 |
GeneticVariation
|
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
rs10210302
|
|
Crohn Disease
|
T |
0.810 |
GeneticVariation
|
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
rs2076756
|
|
Crohn Disease
|
|
0.830 |
GeneticVariation
|
GWASCAT |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |
rs1992660
|
|
Crohn Disease
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
|
17684544 |
2007 |