{{Rsnum
|rsid=2312147
|Chromosome=2
|position=57995793
|Orientation=plus
|GMAF=0.2764
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=VRK2
|Gene_s=VRK2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 29.2 | 55.8 | 15.0
| HCB | 51.1 | 40.1 | 8.8
| JPT | 52.3 | 40.5 | 7.2
| YRI | 91.8 | 8.2 | 0.0
| ASW | 82.5 | 15.8 | 1.8
| CHB | 51.1 | 40.1 | 8.8
| CHD | 47.2 | 39.8 | 13.0
| GIH | 35.6 | 48.5 | 15.8
| LWK | 95.5 | 4.5 | 0.0
| MEX | 36.2 | 44.8 | 19.0
| MKK | 84.6 | 15.4 | 0.0
| TSI | 51.0 | 41.2 | 7.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19571808
|Trait=Schizophrenia
|Title=Common variants conferring risk of schizophrenia
|RiskAllele=C
|Pval=3E-7
|OR=1.09
|ORtxt=[NR]
|OA=1
}}

{{PMID|21791550|OA=1
}} Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2312147
|overall_frequency_n=96
|overall_frequency_d=128
|overall_frequency=0.75
|n_genomes=50
|n_genomes_annotated=0
|n_haplomes=84
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto
|PMID=23102693
|Title=Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility.
}}

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