{{Rsnum
|rsid=11681930
|Gene=PARD3B
|Chromosome=2
|position=205198574
|Orientation=plus
|GMAF=0.2709
|Gene_s=PARD3B
|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 | 1.8 | 26.5 | 71.7
| HCB | 9.6 | 37.0 | 53.3
| JPT | 14.2 | 39.8 | 46.0
| YRI | 11.0 | 46.6 | 42.5
| ASW | 10.5 | 45.6 | 43.9
| CHB | 9.6 | 37.0 | 53.3
| CHD | 8.4 | 46.7 | 44.9
| GIH | 3.0 | 27.7 | 69.3
| LWK | 13.0 | 42.6 | 44.4
| MEX | 1.7 | 27.6 | 70.7
| MKK | 6.4 | 41.0 | 52.6
| TSI | 2.9 | 29.4 | 67.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23527680
  |Trait=Attention deficit hyperactivity disorder (combined symptoms)
  |Title=Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
  |RiskAllele=A
  |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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}