{{Rsnum
|rsid=10491833
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=9
|Orientation=plus
|position=24720234
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 34.5 | 57.5
| HCB | 2.2 | 27.0 | 70.8
| JPT | 1.8 | 24.8 | 73.5
| YRI | 0.0 | 3.4 | 96.6
| ASW | 5.3 | 14.0 | 80.7
| CHB | 2.2 | 27.0 | 70.8
| CHD | 0.9 | 20.2 | 78.9
| GIH | 5.0 | 20.8 | 74.3
| LWK | 0.0 | 0.9 | 99.1
| MEX | 8.6 | 41.4 | 50.0
| MKK | 0.0 | 7.1 | 92.9
| TSI | 3.9 | 35.3 | 60.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24159190
  |Trait=Serum dimethylarginine levels (symmetric)
  |Title=Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
  |RiskAllele=C
  |Pval=4E-6
  |OR=.11
  |ORtxt=[0.064-0.158] unit decrease
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}