{{Rsnum
|rsid=10861342
|Gene=ALDH1L2
|Chromosome=12
|position=105065019
|Orientation=plus
|GMAF=0.1492
|Gene_s=ALDH1L2
|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 | 0.9 | 18.6 | 80.5
| HCB | 7.3 | 33.6 | 59.1
| JPT | 7.1 | 37.2 | 55.8
| YRI | 0.0 | 13.6 | 86.4
| ASW | 1.8 | 14.0 | 84.2
| CHB | 7.3 | 33.6 | 59.1
| CHD | 1.9 | 33.3 | 64.8
| GIH | 0.0 | 26.7 | 73.3
| LWK | 0.0 | 28.2 | 71.8
| MEX | 3.4 | 25.9 | 70.7
| MKK | 1.9 | 15.4 | 82.7
| TSI | 1.0 | 20.6 | 78.4
| 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=2E-6
  |OR=.25
  |ORtxt=[0.14-0.35] unit increase
  |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}}