rs2981575
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2981575(C;C) |
| Make rs2981575(C;T) |
| Make rs2981575(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 121586602 |
| Gene | FGFR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2981575 |
| dbSNP (classic) | rs2981575 |
| ClinGen | rs2981575 |
| ebi | rs2981575 |
| HLI | rs2981575 |
| Exac | rs2981575 |
| Gnomad | rs2981575 |
| Varsome | rs2981575 |
| LitVar | rs2981575 |
| Map | rs2981575 |
| PheGenI | rs2981575 |
| Biobank | rs2981575 |
| 1000 genomes | rs2981575 |
| hgdp | rs2981575 |
| ensembl | rs2981575 |
| geneview | rs2981575 |
| scholar | rs2981575 |
| rs2981575 | |
| pharmgkb | rs2981575 |
| gwascentral | rs2981575 |
| openSNP | rs2981575 |
| 23andMe | rs2981575 |
| SNPshot | rs2981575 |
| SNPdbe | rs2981575 |
| MSV3d | rs2981575 |
| GWAS Ctlg | rs2981575 |
| GMAF | 0.4633 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21060860
] Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
[PMID 19223389] FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation.
