{{Rsnum
|rsid=2107301
|Gene=VDR
|Chromosome=12
|position=47861787
|Orientation=minus
|GMAF=0.3572
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=VDR
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 55.8 | 36.3 | 8.0
| HCB | 9.5 | 36.5 | 54.0
| JPT | 11.5 | 31.0 | 57.5
| YRI | 77.6 | 21.1 | 1.4
| ASW | 70.2 | 26.3 | 3.5
| CHB | 9.5 | 36.5 | 54.0
| CHD | 11.0 | 37.6 | 51.4
| GIH | 48.5 | 38.6 | 12.9
| LWK | 74.5 | 24.5 | 0.9
| MEX | 53.4 | 36.2 | 10.3
| MKK | 74.4 | 23.1 | 2.6
| TSI | 46.1 | 44.1 | 9.8
| HapMapRevision=28
}}
[[rs2107301]] is a SNP in the vitamin D [[VDR]] receptor gene.

[[rs2107301]](T;T) homozygotes were associated with an ~2.5x higher risk of [[prostate cancer]] compared to homozygote carriers of the more common (C) allele in the 630 Caucasian patients studied.{{PMID|17932346}}

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

{{PMID Auto
|PMID=19454612
|Title=Vitamin D pathway gene variants and prostate cancer risk.
|OA=1
}}

{{PMID Auto
|PMID=19753122
|Title=Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk.
|OA=1
}}

{{PMID Auto
|PMID=19956101
|Title=Overview of the Rapid Response data.
|OA=1
}}

{{PMID Auto
|PMID=21948293
|Title=Vitamin D Receptor Gene Variants and Esophageal Adenocarcinoma Risk: A Population-Based Case-Control Study.
}}

{{PMID Auto
|PMID=22576141
|Title=No association of vitamin D metabolism-related polymorphisms and melanoma risk as well as melanoma prognosis: a case-control study.
|OA=1
}}

{{PMID Auto
|PMID=24381141
|Title=Vitamin D receptor gene polymorphisms and esophageal cancer risk in a Chinese population: a negative study
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}