{{Rsnum
|rsid=4675502
|Gene=PARD3B
|Chromosome=2
|position=205221447
|Orientation=plus
|GMAF=0.433
|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 | 38.1 | 49.6 | 12.4
| HCB | 31.4 | 49.6 | 19.0
| JPT | 36.3 | 38.9 | 24.8
| YRI | 26.5 | 56.5 | 17.0
| ASW | 28.1 | 54.4 | 17.5
| CHB | 31.4 | 49.6 | 19.0
| CHD | 25.7 | 57.8 | 16.5
| GIH | 30.7 | 49.5 | 19.8
| LWK | 25.5 | 49.1 | 25.5
| MEX | 43.9 | 47.4 | 8.8
| MKK | 30.8 | 53.8 | 15.4
| TSI | 31.7 | 47.5 | 20.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22843504
  |Trait=Autism
  |Title=Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
  |RiskAllele=
  |Pval=4E-7
  |OR=1.28
  |ORtxt=[1.16-1.41]
  |OA=1
}}

{{on chip | Illumina Human 1M}}