| GWAS snp
|
| PMID
|
[PMID 21841780]
|
| Trait
|
|
| Title
|
A genome-wide association study identifies two new risk loci for Graves' disease.
|
| Risk Allele
|
A
|
| P-val
|
2E-13
|
| Odds Ratio
|
1.2300 [1.17-1.30]
|
[PMID 16859508
] Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?
[PMID 18556175] Lack of association between Fc receptor-like 3 gene polymorphisms and systemic lupus erythematosus in Chinese population.
[PMID 19050767] Association between polymorphisms of FCRL3, a non-HLA gene, and Behcet's disease in a Chinese population with ophthalmic manifestations.
[PMID 19452015] Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome.
[PMID 23505439] A Refined Study of FCRL Genes from a Genome-Wide Association Study for Graves' Disease
| GWAS snp
|
| PMID
|
[PMID 21833088]
|
| Trait
|
Multiple sclerosis
|
| Title
|
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|
| Risk Allele
|
G
|
| P-val
|
3E-6
|
| Odds Ratio
|
1.08 [1.06-1.09]
|
[PMID 24117236] The Fc receptor-like 3 gene polymorphisms and susceptibility to autoimmune diseases: An updated meta-analysis
[PMID 26051414] FCRL3 gene polymorphisms confer risk for sudden sensorineural hearing loss in a Chinese Han Population
] Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?
