{{Rsnum
|rsid=2238135
|Gene=VDR
|Chromosome=12
|position=47884407
|Orientation=minus
|GMAF=0.2456
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(C;G)
|geno3=(C;C)
|Gene_s=VDR
}}[[rs2238135]] is a SNP in the vitamin D [[VDR]] receptor gene.

[[rs2238135]](G;G) 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=17130574
|Title=Protection from type 1 diabetes by vitamin D receptor haplotypes.
}}

{{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=23189278
|Title=VDR gene single nucleotide polymorphisms and their association with risk of oral cavity carcinoma
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}