The query results for rs11264799 , total 9 literatures
There are some abbreviations existing in the query results. For example, RA is an abbreviation for rheumatoid arthritis, H is an abbreviation for healthy controls...more

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Pubmed_ID Title Country Population

15838509
A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.
Japan Asian

16476711
Epistatic interaction between FCRL3 and NFkappaB1 genes in Spanish patients with rheumatoid arthritis.
Spain European

16859508
Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?
UK European

17179172
FCRL3 promoter 169 CC homozygosity is associated with susceptibility to rheumatoid arthritis in Dutch Caucasians.
Holland European

17200162
Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association.
UK,NewZealand European

20732364
Fc receptor-like 3 gene polymorphisms confer susceptibility to rheumatoid arthritis in a Chinese population.
China Asian

21614018
Non-HLA genes modulate the risk of rheumatoid arthritis associated with HLA-DRB1 in a susceptible North American Native population.
Canada American

22386693
FCRL3 gene polymorphisms contribute to the radiographic severity rather than susceptibility of rheumatoid arthritis.
Korea Asian

23883198
Association of FCRL3 genotypes with susceptibility of Iranian patients to rheumatoid arthritis.
Iran Asian

Risk allele : People who carry this allele have a higher risk of developing rheumatoid arthritis than those without this allele.
Related allele in clinical features : Patients with rheumatoid arthritis who carry this allele have different clinical features (such as RF status, ACCP status, age of onset) compared to those without this allele.
Related allele in pharmacogenomics : Patients with rheumatoid arthritis carry this allele are less responsive to drug treatment than those without this allele.
Related allele in cardiovascular (CV) disease : RA patients with this allele have a higher risk of developing CV events than those without this allele.
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