{{Rsnum
|rsid=6453417
|Gene=ARSB
|Chromosome=5
|position=78814709
|Orientation=plus
|GMAF=0.4715
|Gene_s=ARSB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 35.7 | 42.0 | 22.3
| HCB | 33.8 | 46.3 | 19.9
| JPT | 43.8 | 49.1 | 7.1
| YRI | 6.8 | 33.6 | 59.6
| ASW | 8.9 | 32.1 | 58.9
| CHB | 33.8 | 46.3 | 19.9
| CHD | 39.0 | 48.6 | 12.4
| GIH | 14.9 | 40.6 | 44.6
| LWK | 8.3 | 30.3 | 61.5
| MEX | 31.0 | 39.7 | 29.3
| MKK | 14.2 | 43.2 | 42.6
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23728934
  |Trait=Attention deficit hyperactivity disorder
  |Title=Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.
  |RiskAllele=
  |Pval=5E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}