{{Rsnum
|rsid=887199
|Gene=ARVCF
|Chromosome=22
|position=19974432
|Orientation=plus
|GMAF=0.3416
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ARVCF
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 27.4 | 71.7
| HCB | 26.3 | 39.4 | 34.3
| JPT | 15.9 | 50.4 | 33.6
| YRI | 30.6 | 51.7 | 17.7
| ASW | 30.4 | 51.8 | 17.9
| CHB | 26.3 | 39.4 | 34.3
| CHD | 33.9 | 41.3 | 24.8
| GIH | 8.9 | 38.6 | 52.5
| LWK | 26.6 | 50.5 | 22.9
| MEX | 15.5 | 56.9 | 27.6
| MKK | 13.5 | 50.3 | 36.1
| TSI | 0.0 | 22.8 | 77.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=19508883
|Title=ARVCF single marker and haplotypic association with schizophrenia
}}

{{PMID Auto
|PMID=18574484
|Title=The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}