{{Rsnum
|rsid=2110166
|Gene=ANO2
|Chromosome=12
|position=5642176
|Orientation=minus
|GMAF=0.08264
|Gene_s=ANO2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 4.4 | 94.7
| HCB | 1.5 | 21.3 | 77.2
| JPT | 0.0 | 13.3 | 86.7
| YRI | 2.0 | 23.1 | 74.8
| ASW | 0.0 | 8.8 | 91.2
| CHB | 1.5 | 21.3 | 77.2
| CHD | 0.9 | 27.5 | 71.6
| GIH | 0.0 | 5.0 | 95.0
| LWK | 1.8 | 27.3 | 70.9
| MEX | 0.0 | 15.5 | 84.5
| MKK | 1.3 | 30.3 | 68.4
| TSI | 0.0 | 7.8 | 92.2
| 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=.56
  |ORtxt=[0.32-0.81] unit decrease
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}