rs16917546
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16917546(C;C) |
| Make rs16917546(C;T) |
| Make rs16917546(T;T) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 10 |
| Position | 62637778 |
| Gene | LOC105378327, ZNF365 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16917546 |
| dbSNP (classic) | rs16917546 |
| ClinGen | rs16917546 |
| ebi | rs16917546 |
| HLI | rs16917546 |
| Exac | rs16917546 |
| Gnomad | rs16917546 |
| Varsome | rs16917546 |
| LitVar | rs16917546 |
| Map | rs16917546 |
| PheGenI | rs16917546 |
| Biobank | rs16917546 |
| 1000 genomes | rs16917546 |
| hgdp | rs16917546 |
| ensembl | rs16917546 |
| geneview | rs16917546 |
| scholar | rs16917546 |
| rs16917546 | |
| pharmgkb | rs16917546 |
| gwascentral | rs16917546 |
| openSNP | rs16917546 |
| 23andMe | rs16917546 |
| SNPshot | rs16917546 |
| SNPdbe | rs16917546 |
| MSV3d | rs16917546 |
| GWAS Ctlg | rs16917546 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 28177523] Association between genetic variation within vitamin D receptor-DNA binding sites and risk of basal cell carcinoma.
