{{Rsnum
|rsid=2291299
|Gene=C17orf66
|Chromosome=17
|position=35864402
|Orientation=minus
|GMAF=0.2833
|Gene_s=C17orf66
|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 | 71.7 | 25.7 | 2.7
| HCB | 42.6 | 41.9 | 15.4
| JPT | 49.6 | 41.6 | 8.8
| YRI | 27.2 | 53.1 | 19.7
| ASW | 33.3 | 54.4 | 12.3
| CHB | 42.6 | 41.9 | 15.4
| CHD | 52.3 | 41.3 | 6.4
| GIH | 49.5 | 43.6 | 6.9
| LWK | 25.5 | 52.7 | 21.8
| MEX | 51.7 | 37.9 | 10.3
| MKK | 33.3 | 48.7 | 17.9
| TSI | 70.6 | 27.5 | 2.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=23188791
|Title=Genetic polymorphisms associated carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study
|OA=1
}}

{{PMID Auto
|PMID=20041166
|Title=Common genetic variation and the control of HIV-1 in humans.
|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}}