{{Rsnum
|rsid=705117
|Gene=GC
|Chromosome=4
|position=71742398
|Orientation=minus
|GMAF=0.4109
|Gene_s=GC
|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 | 68.1 | 29.2 | 2.7
| HCB | 29.2 | 49.6 | 21.2
| JPT | 18.6 | 48.7 | 32.7
| YRI | 4.1 | 23.1 | 72.8
| ASW | 7.1 | 44.6 | 48.2
| CHB | 29.2 | 49.6 | 21.2
| CHD | 29.4 | 52.3 | 18.3
| GIH | 62.4 | 32.7 | 5.0
| LWK | 1.8 | 22.7 | 75.5
| MEX | 53.4 | 37.9 | 8.6
| MKK | 8.3 | 40.4 | 51.3
| TSI | 61.8 | 34.3 | 3.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=23505139
|Title=An analysis of the association between the vitamin D pathway and serum 25-hydroxyvitamin D levels in a healthy Chinese population
}}

{{PMID Auto
|PMID=18593774
|Title=Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans.
|OA=1
}}

{{PMID Auto
|PMID=19255064
|Title=Vitamin D-related genes, serum vitamin D concentrations and prostate cancer risk.
|OA=1
}}

{{PMID Auto
|PMID=19543766
|Title=Association analyses of vitamin D-binding protein gene with compression strength index variation in Caucasian nuclear families.
|OA=1
}}

{{PMID Auto
|PMID=22785457
|Title=Association of vitamin D-related gene polymorphisms with manifestation of vitamin D deficiency in children.
}}

{{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}}