{{Rsnum
|rsid=1349882
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=2
|Orientation=plus
|position=52722180
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 32.7 | 47.8 | 19.5
| HCB | 27.0 | 53.3 | 19.7
| JPT | 31.0 | 43.4 | 25.7
| YRI | 24.5 | 49.7 | 25.9
| ASW | 26.3 | 45.6 | 28.1
| CHB | 27.0 | 53.3 | 19.7
| CHD | 23.9 | 50.5 | 25.7
| GIH | 44.0 | 44.0 | 12.0
| LWK | 24.5 | 47.3 | 28.2
| MEX | 53.4 | 31.0 | 15.5
| MKK | 17.4 | 46.5 | 36.1
| TSI | 31.4 | 51.0 | 17.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24159190
  |Trait=Serum dimethylarginine levels (asymmetric)
  |Title=Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
  |RiskAllele=T
  |Pval=5E-6
  |OR=.09
  |ORtxt=[0.053-0.131] unit increase
  }}

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