{{Rsnum
|rsid=667773
|Gene=PAX6
|Chromosome=11
|position=31793814
|Orientation=minus
|GMAF=0.09183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PAX6
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 90.3 | 8.8 | 0.9
| HCB | 68.4 | 26.5 | 5.1
| JPT | 77.9 | 21.2 | 0.9
| YRI | 92.5 | 7.5 | 0.0
| ASW | 89.3 | 10.7 | 0.0
| CHB | 68.4 | 26.5 | 5.1
| CHD | 63.3 | 34.9 | 1.8
| GIH | 91.1 | 8.9 | 0.0
| LWK | 86.4 | 12.7 | 0.9
| MEX | 65.5 | 34.5 | 0.0
| MKK | 73.7 | 24.4 | 1.9
| TSI | 88.2 | 11.8 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19607881
|Title=A novel missense mutation (Leu46Val) of PAX6 found in an autistic patient
}}

{{PMID|15307048|OA=1
}} A susceptibility locus for myopia in the normal population is linked to the PAX6 gene region on chromosome 11: a genomewide scan of dizygotic twins.

{{PMID|17948041}} A PAX6 gene polymorphism is associated with genetic predisposition to extreme myopia.

{{PMID|19142206|OA=1
}} Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations.

{{PMID|19907666|OA=1
}} AC and AG dinucleotide repeats in the PAX6 P1 promoter are associated with high myopia.

{{PMID|21348901}} PAX6 polymorphisms in 20 Chinese children with supernumerary teeth in the maxillary incisor area.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}