rs2189480
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2189480(A;A) |
| Make rs2189480(A;C) |
| Make rs2189480(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 47870045 |
| Gene | VDR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2189480 |
| dbSNP (classic) | rs2189480 |
| ClinGen | rs2189480 |
| ebi | rs2189480 |
| HLI | rs2189480 |
| Exac | rs2189480 |
| Gnomad | rs2189480 |
| Varsome | rs2189480 |
| LitVar | rs2189480 |
| Map | rs2189480 |
| PheGenI | rs2189480 |
| Biobank | rs2189480 |
| 1000 genomes | rs2189480 |
| hgdp | rs2189480 |
| ensembl | rs2189480 |
| geneview | rs2189480 |
| scholar | rs2189480 |
| rs2189480 | |
| pharmgkb | rs2189480 |
| gwascentral | rs2189480 |
| openSNP | rs2189480 |
| 23andMe | rs2189480 |
| SNPshot | rs2189480 |
| SNPdbe | rs2189480 |
| MSV3d | rs2189480 |
| GWAS Ctlg | rs2189480 |
| GMAF | 0.4403 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 23413917
] Serum 25-hydroxyvitamin D3 levels and vitamin D receptor variants in melanoma patients from the Mediterranean area of Barcelona: 25-hydroxyvitamin D3 levels and VDR variants in melanoma patients from Barcelona
[PMID 17903296
] Genome-wide association with bone mass and geometry in the Framingham Heart Study.
[PMID 19956101
] Overview of the Rapid Response data.
[PMID 19956103
] Association analyses of the vitamin D receptor gene in 1654 families with type I diabetes.
[PMID 30683435] Serum vitamin D deficiency and vitamin D receptor gene polymorphism are associated with increased risk of cardiovascular disease in a Chinese rural population.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 12
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2c
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2d
