{{Rsnum
|rsid=1515641
|Gene=LOC728586
|Chromosome=5
|position=127803924
|Orientation=plus
|GMAF=0.1056
|Gene_s=LOC728586
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 1.8 | 98.2
| HCB | 3.6 | 35.0 | 61.3
| JPT | 8.0 | 34.5 | 57.5
| YRI | 0.0 | 15.6 | 84.4
| ASW | 0.0 | 12.3 | 87.7
| CHB | 3.6 | 35.0 | 61.3
| CHD | 9.2 | 37.6 | 53.2
| GIH | 0.0 | 8.9 | 91.1
| LWK | 1.8 | 20.0 | 78.2
| MEX | 3.4 | 31.0 | 65.5
| MKK | 2.6 | 14.1 | 83.3
| TSI | 0.0 | 2.0 | 98.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23527680
  |Trait=Attention deficit hyperactivity disorder (hyperactivity-impulsivity symptoms)
  |Title=Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
  |RiskAllele=A
  |Pval=4E-6
  |OR=NR
  |ORtxt=NR
  }}

{{PMID Auto
|PMID=17903302
|Title=Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.
|OA=1
}}

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