{{Rsnum
|rsid=1319535
|Gene=LINGO2
|Chromosome=9
|position=28181087
|Orientation=plus
|GMAF=0.4128
|Gene_s=LINGO2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 14.4 | 37.8 | 47.7
| HCB | 20.9 | 47.0 | 32.1
| JPT | 37.3 | 48.2 | 14.5
| YRI | 14.4 | 44.5 | 41.1
| ASW | 22.8 | 42.1 | 35.1
| CHB | 20.9 | 47.0 | 32.1
| CHD | 15.6 | 54.1 | 30.3
| GIH | 46.4 | 39.2 | 14.4
| LWK | 6.4 | 38.2 | 55.5
| MEX | 6.9 | 50.0 | 43.1
| MKK | 8.1 | 44.3 | 47.7
| TSI | 14.7 | 46.1 | 39.2
| 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=9E-6
  |OR=.15
  |ORtxt=[0.081-0.21] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}