rs10736303
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10736303(A;A) |
| Make rs10736303(A;G) |
| Make rs10736303(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 121574943 |
| Gene | FGFR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10736303 |
| dbSNP (classic) | rs10736303 |
| ClinGen | rs10736303 |
| ebi | rs10736303 |
| HLI | rs10736303 |
| Exac | rs10736303 |
| Gnomad | rs10736303 |
| Varsome | rs10736303 |
| LitVar | rs10736303 |
| Map | rs10736303 |
| PheGenI | rs10736303 |
| Biobank | rs10736303 |
| 1000 genomes | rs10736303 |
| hgdp | rs10736303 |
| ensembl | rs10736303 |
| geneview | rs10736303 |
| scholar | rs10736303 |
| rs10736303 | |
| pharmgkb | rs10736303 |
| gwascentral | rs10736303 |
| openSNP | rs10736303 |
| 23andMe | rs10736303 |
| SNPshot | rs10736303 |
| SNPdbe | rs10736303 |
| MSV3d | rs10736303 |
| GWAS Ctlg | rs10736303 |
| GMAF | 0.3774 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22452962
] A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study
[PMID 18285324] Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk.
[PMID 19223389] FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation.
[PMID 19497954] Histone-acetylated control of fibroblast growth factor receptor 2 intron 2 polymorphisms and isoform splicing in breast cancer.
