{{Rsnum
|rsid=2239185
|Gene=VDR
|Chromosome=12
|position=47850776
|Orientation=minus
|GMAF=0.4803
|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 | 0.0 | 0.0 | 0.0
| HCB | 53.3 | 33.3 | 13.3
| JPT | 32.6 | 55.8 | 11.6
| YRI | 20.6 | 49.2 | 30.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 53.3 | 33.3 | 13.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PharmGKB
|RSID=rs2239185
|Name_s=
|Gene_s=VDR
|Feature=
|Evidence=Web Resource:http://www.pharmgkb.org/search/annotatedGene/vdr/variant.jsp
|Annotation=Associated with susceptibility to asthma and with IgE levels.
|Drugs=
|Drug Classes=
|Diseases=Asthma
|Curation Level=In-Depth
|PharmGKB Accession ID=PA161145148
}}

{{PMID Auto
|PMID=15651992
|Title=Variants in the vitamin D receptor gene and asthma.
|OA=1
}}

{{PMID Auto
|PMID=16600026
|Title=Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathway.
|OA=1
}}

{{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=18936436
|Title=Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.
|OA=1
}}

{{PMID Auto
|PMID=19622139
|Title=Association study between vitamin D receptor gene polymorphisms and asthma in the Chinese Han population: a case-control study.
|OA=1
}}

{{PMID Auto
|PMID=19745160
|Title=Trend tests for genetic association using population-based cross-sectional complex survey data.
}}

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

{{PMID Auto
|PMID=20006704
|Title=Lead and cognitive function in VDR genotypes in the third National Health and Nutrition Examination Survey.
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2239185
|overall_frequency_n=63
|overall_frequency_d=118
|overall_frequency=0.533898
|n_genomes=36
|n_genomes_annotated=0
|n_haplomes=49
|n_articles=0
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}