{{Rsnum
|rsid=6537825
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TRIM33
|position=114405659
|Gene_s=LOC101928890,TRIM33
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 14.2 | 85.0
| HCB | 15.3 | 48.2 | 36.5
| JPT | 13.4 | 40.2 | 46.4
| YRI | 0.0 | 3.4 | 96.6
| ASW | 0.0 | 1.8 | 98.2
| CHB | 15.3 | 48.2 | 36.5
| CHD | 21.1 | 49.5 | 29.4
| GIH | 2.0 | 11.9 | 86.1
| LWK | 0.0 | 3.6 | 96.4
| MEX | 3.4 | 36.2 | 60.3
| MKK | 0.0 | 7.1 | 92.9
| TSI | 0.0 | 15.7 | 84.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24189344
  |Trait=Autism
  |Title=Common genetic variants on 1p13.2 associate with risk of autism.
  |RiskAllele=A
  |Pval=3E-8
  |OR=1.40
  |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}}