{{Rsnum
|rsid=945635
|Gene=FCRL3
|Chromosome=1
|position=157700500
|Orientation=plus
|GMAF=0.4444
|Gene_s=FCRL3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 28.6 | 58.7 | 12.7
| HCB | 40.0 | 46.7 | 13.3
| JPT | 29.5 | 43.2 | 27.3
| YRI | 0.0 | 16.1 | 83.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 40.0 | 46.7 | 13.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24117236
|Title=The Fc receptor-like 3 gene polymorphisms and susceptibility to autoimmune diseases: An updated meta-analysis
}}

{{PMID Auto
|PMID=16859508
|Title=Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?
|OA=1
}}

{{PMID Auto
|PMID=18556175
|Title=Lack of association between Fc receptor-like 3 gene polymorphisms and systemic lupus erythematosus in Chinese population.
}}

{{PMID Auto
|PMID=19050767
|Title=Association between polymorphisms of FCRL3, a non-HLA gene, and Behcet's disease in a Chinese population with ophthalmic manifestations.
|OA=1
}}

{{PMID Auto
|PMID=19452015
|Title=Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome.
|OA=1
}}

{{PMID Auto
|PMID=19877046
|Title=The FCRL3-169CT promoter single-nucleotide polymorphism, which is associated with systemic lupus erythematosus in a Japanese population, predicts expression of receptor protein on CD19+ B cells.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}