{{Rsnum
|rsid=707916
|Gene=DDAH2
|Chromosome=6
|position=31729781
|Orientation=minus
|GMAF=0.4738
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DDAH2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 52.7 | 39.3 | 8.0
| HCB | 30.9 | 50.0 | 19.1
| JPT | 32.7 | 45.1 | 22.1
| YRI | 4.1 | 18.4 | 77.6
| ASW | 7.0 | 40.4 | 52.6
| CHB | 30.9 | 50.0 | 19.1
| CHD | 33.9 | 48.6 | 17.4
| GIH | 31.7 | 53.5 | 14.9
| LWK | 12.8 | 34.9 | 52.3
| MEX | 29.8 | 54.4 | 15.8
| MKK | 10.3 | 46.2 | 43.6
| TSI | 39.2 | 46.1 | 14.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=19250061
|Title=Common genetic variation in DDAH2 is associated with intracerebral hemorrhage in Chinese population: a multicenter case-control study in China.
}}

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