{{Rsnum
|rsid=4238010
|Chromosome=12
|position=4009151
|Orientation=plus
|GMAF=0.1354
|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 | 77.9 | 22.1 | 0.0
| HCB | 89.1 | 10.9 | 0.0
| JPT | 91.2 | 8.8 | 0.0
| YRI | 42.2 | 49.0 | 8.8
| ASW | 64.9 | 29.8 | 5.3
| CHB | 89.1 | 10.9 | 0.0
| CHD | 89.9 | 10.1 | 0.0
| GIH | 87.1 | 11.9 | 1.0
| LWK | 37.3 | 50.0 | 12.7
| MEX | 91.4 | 8.6 | 0.0
| MKK | 53.2 | 38.5 | 8.3
| TSI | 88.2 | 10.8 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19107115
|Trait=Major depressive disorder
|Title=Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts
|RiskAllele=G
|Pval=0.000006
|OR=1.72
|ORtxt=None
}}

{{PharmGKB
|RSID=rs4238010
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19107115; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts. (Initial Sample Size: 1,359 cases, 1,782 controls; Replication Sample Size: NR); (Region: 12p13.32; Reported Gene(s): CCND2; Risk Allele: rs4238010-G); (p-value= 0.000006).This variant is associated with Major depressive disorder.
|Drugs=
|Drug Classes=
|Diseases=Depression
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740101
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4238010
|overall_frequency_n=106
|overall_frequency_d=128
|overall_frequency=0.828125
|n_genomes=52
|n_genomes_annotated=0
|n_haplomes=92
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}