{{Rsnum
|rsid=7633075
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=3
|Orientation=plus
|Gene=NPM1P3
|position=18540356
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC101927777
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 77.9 | 21.2 | 0.9
| HCB | 38.5 | 48.9 | 12.6
| JPT | 31.9 | 47.8 | 20.4
| YRI | 30.1 | 47.9 | 21.9
| ASW | 28.1 | 47.4 | 24.6
| CHB | 38.5 | 48.9 | 12.6
| CHD | 46.3 | 41.7 | 12.0
| GIH | 66.3 | 30.7 | 3.0
| LWK | 35.5 | 46.4 | 18.2
| MEX | 32.8 | 46.6 | 20.7
| MKK | 32.7 | 41.7 | 25.6
| TSI | 74.5 | 24.5 | 1.0
| 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=T
  |Pval=6E-6
  |OR=.13
  |ORtxt=[0.076-0.19] unit decrease
  }}

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