rs146217902
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs146217902(A;A) |
| Make rs146217902(A;G) |
| Make rs146217902(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 5215887 |
| Gene | EDEM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs146217902 |
| dbSNP (classic) | rs146217902 |
| ClinGen | rs146217902 |
| ebi | rs146217902 |
| HLI | rs146217902 |
| Exac | rs146217902 |
| Gnomad | rs146217902 |
| Varsome | rs146217902 |
| LitVar | rs146217902 |
| Map | rs146217902 |
| PheGenI | rs146217902 |
| Biobank | rs146217902 |
| 1000 genomes | rs146217902 |
| hgdp | rs146217902 |
| ensembl | rs146217902 |
| geneview | rs146217902 |
| scholar | rs146217902 |
| rs146217902 | |
| pharmgkb | rs146217902 |
| gwascentral | rs146217902 |
| openSNP | rs146217902 |
| 23andMe | rs146217902 |
| SNPshot | rs146217902 |
| SNPdbe | rs146217902 |
| MSV3d | rs146217902 |
| GWAS Ctlg | rs146217902 |
| Max Magnitude | 0 |
[PMID 24470074
] Rare coding variants and breast cancer risk: Evaluation of susceptibility loci identified in genome-wide association studies
