{{Rsnum
|rsid=12230513
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OR6C64P
|position=55522996
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 73.5 | 20.4 | 6.2
| HCB | 31.4 | 49.6 | 19.0
| JPT | 40.7 | 52.2 | 7.1
| YRI | 88.4 | 10.2 | 1.4
| ASW | 80.7 | 17.5 | 1.8
| CHB | 31.4 | 49.6 | 19.0
| CHD | 30.3 | 54.1 | 15.6
| GIH | 81.2 | 16.8 | 2.0
| LWK | 82.6 | 17.4 | 0.0
| MEX | 70.7 | 27.6 | 1.7
| MKK | 59.6 | 33.3 | 7.1
| TSI | 67.6 | 29.4 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24152035
  |Trait=Contrast sensitivity
  |Title=Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia.
  |RiskAllele=
  |Pval=5E-6
  |OR=2.69
  |ORtxt=[NR] unit decrease
  }}

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