{{Rsnum
|rsid=6538761
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|position=97040442
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 14.2 | 48.7 | 37.2
| HCB | 25.5 | 48.2 | 26.3
| JPT | 35.4 | 46.9 | 17.7
| YRI | 9.5 | 34.0 | 56.5
| ASW | 3.5 | 52.6 | 43.9
| CHB | 25.5 | 48.2 | 26.3
| CHD | 24.8 | 48.6 | 26.6
| GIH | 14.9 | 43.6 | 41.6
| LWK | 7.3 | 50.0 | 42.7
| MEX | 6.9 | 51.7 | 41.4
| MKK | 9.0 | 51.0 | 40.0
| TSI | 9.8 | 48.0 | 42.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24189344
  |Trait=Autism
  |Title=Common genetic variants on 1p13.2 associate with risk of autism.
  |RiskAllele=A
  |Pval=2E-6
  |OR=1.24
  |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}}