rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
The T300A Crohn's disease risk polymorphism impairs function of the WD40 domain of ATG16L1.
|
27273576 |
2016 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
The Thr300Ala variant in ATG16L1 is associated with improved survival in human colorectal cancer and enhanced production of type I interferon.
|
25645662 |
2016 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
Autophagy genes variants and paediatric Crohn's disease phenotype: a single-centre experience.
|
24656308 |
2014 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
A Crohn's disease variant in Atg16l1 enhances its degradation by caspase 3.
|
24553140 |
2014 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
Autophagy 16-like 1 rs2241880 G allele is associated with Crohn's disease in German children.
|
19659808 |
2009 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
Autophagy gene ATG16L1 but not IRGM is associated with Crohn's disease in Canadian children.
|
18985712 |
2009 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
ATG16L1 and IL23 receptor (IL23R) genes are associated with disease susceptibility in Hungarian CD patients.
|
18499543 |
2008 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
ATG16L1 and IL23R are associated with inflammatory bowel diseases but not with celiac disease in the Netherlands.
|
18047540 |
2008 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.
|
17484864 |
2007 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
|
17435756 |
2007 |
rs2241880
|
ATG16L1;SCARNA5
|
Inflammatory Bowel Disease 10
|
|
0.700 |
GeneticVariation |
UNIPROT |
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
|
17200669 |
2007 |