rs1459015
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1459015(A;A) |
| Make rs1459015(A;G) |
| Make rs1459015(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 13500728 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1459015 |
| dbSNP (classic) | rs1459015 |
| ClinGen | rs1459015 |
| ebi | rs1459015 |
| HLI | rs1459015 |
| Exac | rs1459015 |
| Gnomad | rs1459015 |
| Varsome | rs1459015 |
| LitVar | rs1459015 |
| Map | rs1459015 |
| PheGenI | rs1459015 |
| Biobank | rs1459015 |
| 1000 genomes | rs1459015 |
| hgdp | rs1459015 |
| ensembl | rs1459015 |
| geneview | rs1459015 |
| scholar | rs1459015 |
| rs1459015 | |
| pharmgkb | rs1459015 |
| gwascentral | rs1459015 |
| openSNP | rs1459015 |
| 23andMe | rs1459015 |
| SNPshot | rs1459015 |
| SNPdbe | rs1459015 |
| MSV3d | rs1459015 |
| GWAS Ctlg | rs1459015 |
| Max Magnitude | 0 |
[PMID 26339419
] Association between promoter region genetic variants of PTH SNPs and serum 25(OH)-vitamin D level
