{{Rsnum
|rsid=469568
|Gene=ADAMTS2
|Chromosome=5
|position=179236407
|Orientation=plus
|GMAF=0.4141
|Gene_s=ADAMTS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 33.6 | 46.0 | 20.4
| HCB | 0.0 | 8.8 | 91.2
| JPT | 0.0 | 15.0 | 85.0
| YRI | 31.3 | 53.7 | 15.0
| ASW | 38.6 | 43.9 | 17.5
| CHB | 0.0 | 8.8 | 91.2
| CHD | 0.9 | 8.3 | 90.8
| GIH | 13.0 | 50.0 | 37.0
| LWK | 35.2 | 52.8 | 12.0
| MEX | 12.1 | 46.6 | 41.4
| MKK | 40.0 | 46.5 | 13.5
| TSI | 20.6 | 57.8 | 21.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22990015
  |Trait=Stroke (pediatric)
  |Title=A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.
  |RiskAllele=T
  |Pval=8E-6
  |OR=1.77
  |ORtxt=[NR]
  }}

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