{{Rsnum
|rsid=10838524
|Gene=CRY2
|Chromosome=11
|position=45848626
|Orientation=plus
|GMAF=0.3453
|Gene_s=CRY2
|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 | 22.1 | 53.1 | 24.8
| HCB | 59.9 | 36.5 | 3.6
| JPT | 60.2 | 38.1 | 1.8
| YRI | 91.2 | 8.2 | 0.7
| ASW | 71.9 | 24.6 | 3.5
| CHB | 59.9 | 36.5 | 3.6
| CHD | 57.8 | 34.9 | 7.3
| GIH | 22.8 | 48.5 | 28.7
| LWK | 93.6 | 6.4 | 0.0
| MEX | 19.3 | 56.1 | 24.6
| MKK | 82.7 | 14.7 | 2.6
| TSI | 14.7 | 56.9 | 28.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=23138696
|Title=Association of Tef polymorphism with depression in Parkinson disease
}}

{{PMID Auto
|PMID=20174623
|Title=Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance.
|OA=1
}}

{{PMID Auto
|PMID=20195522
|Title=CRY2 is associated with depression.
|OA=1
}}

{{PMID Auto
|PMID=22538398
|Title=Clock gene variants in mood and anxiety disorders.
}}

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