{{Rsnum
|rsid=2381628
|Gene=FCRL6
|Chromosome=9
|position=7518656
|Orientation=plus
|GMAF=0.2052
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 69.9 | 28.3 | 1.8
| HCB | 94.2 | 5.1 | 0.7
| JPT | 95.6 | 4.4 | 0.0
| YRI | 39.5 | 45.6 | 15.0
| ASW | 31.6 | 49.1 | 19.3
| CHB | 94.2 | 5.1 | 0.7
| CHD | 89.0 | 9.2 | 1.8
| GIH | 87.1 | 11.9 | 1.0
| LWK | 27.3 | 50.9 | 21.8
| MEX | 70.7 | 27.6 | 1.7
| MKK | 33.3 | 50.0 | 16.7
| TSI | 58.8 | 36.3 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=C
  |Pval=6E-6
  |OR=.18
  |ORtxt=[0.1-0.26] unit increase
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}