rs2245092
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2245092(A;A) |
| Make rs2245092(A;G) |
| Make rs2245092(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 62613713 |
| Gene | TLK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2245092 |
| dbSNP (classic) | rs2245092 |
| ClinGen | rs2245092 |
| ebi | rs2245092 |
| HLI | rs2245092 |
| Exac | rs2245092 |
| Gnomad | rs2245092 |
| Varsome | rs2245092 |
| LitVar | rs2245092 |
| Map | rs2245092 |
| PheGenI | rs2245092 |
| Biobank | rs2245092 |
| 1000 genomes | rs2245092 |
| hgdp | rs2245092 |
| ensembl | rs2245092 |
| geneview | rs2245092 |
| scholar | rs2245092 |
| rs2245092 | |
| pharmgkb | rs2245092 |
| gwascentral | rs2245092 |
| openSNP | rs2245092 |
| 23andMe | rs2245092 |
| SNPshot | rs2245092 |
| SNPdbe | rs2245092 |
| MSV3d | rs2245092 |
| GWAS Ctlg | rs2245092 |
| GMAF | 0.3315 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19454617
] Genetic variation in the chromosome 17q23 amplicon and breast cancer risk
