{{Rsnum
|rsid=6885224
|Gene=CTNND2
|Chromosome=5
|position=11169833
|Orientation=plus
|GMAF=0.3471
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CTNND2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 12.8 | 55.0 | 32.1
| HCB | 5.1 | 38.7 | 56.2
| JPT | 3.6 | 33.0 | 63.4
| YRI | 1.4 | 23.8 | 74.8
| ASW | 5.3 | 24.6 | 70.2
| CHB | 5.1 | 38.7 | 56.2
| CHD | 5.5 | 33.0 | 61.5
| GIH | 25.0 | 48.0 | 27.0
| LWK | 2.7 | 29.1 | 68.2
| MEX | 26.3 | 52.6 | 21.1
| MKK | 3.8 | 30.8 | 65.4
| TSI | 22.5 | 48.0 | 29.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21095009
|Trait=None
|Title=Genome-Wide Association Studies Reveal Genetic Variants in CTNND2 for High Myopia in Singapore Chinese
|RiskAllele=C
|Pval=0.000008
|OR=1.2400
|ORtxt=[1.11-1.39]
|OA=1
}}

{{PMID Auto
|PMID=21911587
|Title=Replication study supports CTNND2 as a susceptibility gene for high myopia.
}}

{{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}}