| OMIM | 612009 |
| Desc | CELIAC DISEASE, SUSCEPTIBILITY TO, 11; CELIAC11 |
| Variant | |
| Related | also |
[PMID 19693089] Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort
| GWAS snp
|
| PMID
|
[PMID 20190752 ]
|
| Trait
|
Celiac disease
|
| Title
|
Multiple common variants for celiac disease influencing immune gene expression
|
| Risk Allele
|
A
|
| P-val
|
3E-40
|
| Odds Ratio
|
1.29 [1.25-1.34]
|
| GWAS snp
|
| PMID
|
[PMID 20410501]
|
| Trait
|
Vitiligo
|
| Title
|
Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo
|
| Risk Allele
|
T
|
| P-val
|
1E-11
|
| Odds Ratio
|
1.31 [1.21-1.41]
|
[PMID 22087237] Improving the estimation of celiac disease sibling risk by non-HLA genes
[PMID 18853133] Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes.
[PMID 19073967] Shared and distinct genetic variants in type 1 diabetes and celiac disease.
[PMID 20647273] Investigation of type 1 diabetes and coeliac disease susceptibility loci for association with juvenile idiopathic arthritis.
[PMID 22922229] Seven newly identified loci for autoimmune thyroid disease.
]
