rs7139166
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7139166(C;C) |
| Make rs7139166(C;G) |
| Make rs7139166(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 47906551 |
| Gene | VDR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7139166 |
| dbSNP (classic) | rs7139166 |
| ClinGen | rs7139166 |
| ebi | rs7139166 |
| HLI | rs7139166 |
| Exac | rs7139166 |
| Gnomad | rs7139166 |
| Varsome | rs7139166 |
| LitVar | rs7139166 |
| Map | rs7139166 |
| PheGenI | rs7139166 |
| Biobank | rs7139166 |
| 1000 genomes | rs7139166 |
| hgdp | rs7139166 |
| ensembl | rs7139166 |
| geneview | rs7139166 |
| scholar | rs7139166 |
| rs7139166 | |
| pharmgkb | rs7139166 |
| gwascentral | rs7139166 |
| openSNP | rs7139166 |
| 23andMe | rs7139166 |
| SNPshot | rs7139166 |
| SNPdbe | rs7139166 |
| MSV3d | rs7139166 |
| GWAS Ctlg | rs7139166 |
| GMAF | 0.2149 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20046590
] The unfavorable effect of the A allele of the vitamin D receptor promoter polymorphism A-1012G has different mechanisms related to susceptibility and outcome of malignant melanoma
[PMID 21365644] Vitamin D receptor polymorphisms in patients with cutaneous melanoma
[PMID 18828731] Vitamin D receptor gene polymorphisms have negligible effect on human height.
