{{Rsnum
|rsid=738144
|Gene=DNAL4
|Chromosome=22
|position=38782370
|Orientation=plus
|GMAF=0.1483
|Gene_s=DNAL4
|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 | 61.1 | 35.4 | 3.5
| HCB | 86.1 | 13.1 | 0.7
| JPT | 82.3 | 14.2 | 3.5
| YRI | 78.9 | 18.4 | 2.7
| ASW | 89.5 | 10.5 | 0.0
| CHB | 86.1 | 13.1 | 0.7
| CHD | 83.5 | 16.5 | 0.0
| GIH | 70.3 | 28.7 | 1.0
| LWK | 87.3 | 11.8 | 0.9
| MEX | 79.3 | 17.2 | 3.4
| MKK | 82.1 | 17.9 | 0.0
| TSI | 64.7 | 32.4 | 2.9
| 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=G
  |Pval=7E-6
  |OR=.19
  |ORtxt=[0.11-0.27] unit increase
  |OA=1
}}

{{on chip | Illumina Human 1M}}