{{Rsnum
|rsid=7834018
|Chromosome=8
|position=71649507
|Orientation=plus
|GMAF=0.2557
|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 | 0.9 | 16.8 | 82.3
| HCB | 12.4 | 51.1 | 36.5
| JPT | 17.9 | 48.2 | 33.9
| YRI | 8.2 | 43.5 | 48.3
| ASW | 7.0 | 43.9 | 49.1
| CHB | 12.4 | 51.1 | 36.5
| CHD | 11.0 | 51.4 | 37.6
| GIH | 11.9 | 45.5 | 42.6
| LWK | 10.9 | 37.3 | 51.8
| MEX | 13.8 | 41.4 | 44.8
| MKK | 2.6 | 31.4 | 66.0
| TSI | 0.0 | 23.5 | 76.5
| 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=8E-7
  |OR=1.56
  |ORtxt=[1.3-1.89]
  |OA=1
}}

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