{{Rsnum
|rsid=7711337
|Chromosome=5
|position=162656512
|Orientation=plus
|GMAF=0.3402
|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 | 19.6 | 40.2 | 40.2
| HCB | 0.0 | 4.4 | 95.6
| JPT | 0.0 | 3.6 | 96.4
| YRI | 38.8 | 46.3 | 15.0
| ASW | 24.6 | 54.4 | 21.1
| CHB | 0.0 | 4.4 | 95.6
| CHD | 0.0 | 3.7 | 96.3
| GIH | 4.0 | 31.7 | 64.4
| LWK | 31.8 | 49.1 | 19.1
| MEX | 15.5 | 53.4 | 31.0
| MKK | 41.3 | 47.7 | 11.0
| TSI | 17.6 | 49.0 | 33.3
| 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=1.22
  |ORtxt=[1.12-1.32]
  |OA=1
}}

{{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}}