rs112594756
From SNPedia
| Merged into | rs60388563 |
| Orientation | plus |
| Make rs112594756(C;C) |
| Make rs112594756(C;G) |
| Make rs112594756(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 3 |
| Position | 122201839 |
| Gene | CASR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs112594756 |
| dbSNP (classic) | rs112594756 |
| ClinGen | rs112594756 |
| ebi | rs112594756 |
| HLI | rs112594756 |
| Exac | rs112594756 |
| Gnomad | rs112594756 |
| Varsome | rs112594756 |
| LitVar | rs112594756 |
| Map | rs112594756 |
| PheGenI | rs112594756 |
| Biobank | rs112594756 |
| 1000 genomes | rs112594756 |
| hgdp | rs112594756 |
| ensembl | rs112594756 |
| geneview | rs112594756 |
| scholar | rs112594756 |
| rs112594756 | |
| pharmgkb | rs112594756 |
| gwascentral | rs112594756 |
| openSNP | rs112594756 |
| 23andMe | rs112594756 |
| SNPshot | rs112594756 |
| SNPdbe | rs112594756 |
| MSV3d | rs112594756 |
| GWAS Ctlg | rs112594756 |
| Status | Merged into rs60388563 |
| Max Magnitude | 0 |
[PMID 26650177
] Genetic variations in vitamin D-related pathways and breast cancer risk in African American women in the AMBER Consortium.
